Canonical Allele Identifier: CA2580062909
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2453358
ClinVar RCV Id: RCV003182813

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329397_45329407del , CM000663.2:g.45329397_45329407del GRCh38
NC_000001.10:g.45795069_45795079del , CM000663.1:g.45795069_45795079del GRCh37
NC_000001.9:g.45567656_45567666del NCBI36
NG_008189.1:g.16064_16074del , LRG_220:g.16064_16074del

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.1081_1091del ENSP00000410263.2:p.Cys361LysfsTer11
ENST00000435155.2:c.1498_1508del ENSP00000403655.2:p.Cys500LysfsTer11
ENST00000467459.6:c.*327_*337del ENSP00000435889.2:n.*327_*337del
ENST00000483127.2:c.1483_1493del ENSP00000436469.2:p.Cys495LysfsTer11
ENST00000485271.6:c.*208_*218del ENSP00000431264.2:n.*208_*218del
ENST00000529892.6:c.1318_1328del ENSP00000432528.2:p.Cys440LysfsTer11
ENST00000533178.6:c.*794_*804del ENSP00000436430.2:n.*794_*804del
ENST00000672314.2:c.1465_1475del ENSP00000500828.2:p.Cys489LysfsTer11
ENST00000710952.2:c.1549_1559del MANE Plus Clinical ENSP00000518552.2:p.Cys517LysfsTer11
ENST00000672818.3:c.1540_1550del ENSP00000500891.1:p.Cys514LysfsTer11
ENST00000456914.7:c.1465_1475del MANE Select ENSP00000407590.2:p.Cys489LysfsTer11
ENST00000671898.1:c.*208_*218del ENSP00000499896.1:n.*208_*218del
ENST00000672011.1:c.*794_*804del ENSP00000500418.1:n.*794_*804del
ENST00000672818.2:c.1540_1550del ENSP00000500891.1:p.Cys514LysfsTer11
ENST00000354383.10:c.1468_1478del ENSP00000346354.6:p.Cys490LysfsTer11
ENST00000355498.6:c.1465_1475del ENSP00000347685.2:p.Cys489LysfsTer11
ENST00000372098.7:c.1540_1550del ENSP00000361170.3:p.Cys514LysfsTer11
ENST00000372104.5:c.1465_1475del ENSP00000361176.1:p.Cys489LysfsTer11
ENST00000372110.7:c.1510_1520del ENSP00000361182.3:p.Cys504LysfsTer11
ENST00000372115.7:c.1507_1517del ENSP00000361187.3:p.Cys503LysfsTer11
ENST00000448481.5:c.1498_1508del ENSP00000409718.1:p.Cys500LysfsTer11
ENST00000450313.5:c.1549_1559del ENSP00000408176.1:p.Cys517LysfsTer11
ENST00000456914.6:c.1465_1475del ENSP00000407590.2:p.Cys489LysfsTer11
ENST00000467459.5:c.882_892del ENSP00000435889.1:n.882_892del
ENST00000475516.5:c.*1278_*1288del ENSP00000433843.1:n.*1278_*1288del
ENST00000481571.5:c.*1278_*1288del ENSP00000436597.1:n.*1278_*1288del
ENST00000482094.5:n.786_796del
ENST00000485271.5:c.342_352del
ENST00000488731.6:c.550_560del ENSP00000432330.1:p.Cys184LysfsTer11
ENST00000528013.6:c.1507_1517del ENSP00000433130.2:p.Cys503LysfsTer11
ENST00000529892.5:c.540_550del
ENST00000529984.5:c.550_560del ENSP00000437093.1:p.Cys184LysfsTer11
ENST00000531105.5:c.146_156del ENSP00000431292.1:p.Val49GlufsTer?
ENST00000533178.5:c.1094_1104del ENSP00000436430.1:n.1094_1104del
NM_001048171.1:c.1507_1517del NP_001041636.1:p.Cys503LysfsTer11
NM_001048172.1:c.1468_1478del NP_001041637.1:p.Cys490LysfsTer11
NM_001048173.1:c.1465_1475del NP_001041638.1:p.Cys489LysfsTer11
NM_001048174.1:c.1465_1475del NP_001041639.1:p.Cys489LysfsTer11
NM_001128425.1:c.1549_1559del , LRG_220t1:c.1549_1559del NP_001121897.1:p.Cys517LysfsTer11
NM_001293190.1:c.1510_1520del NP_001280119.1:p.Cys504LysfsTer11
NM_001293191.1:c.1498_1508del NP_001280120.1:p.Cys500LysfsTer11
NM_001293192.1:c.1189_1199del NP_001280121.1:p.Cys397LysfsTer11
NM_001293195.1:c.1465_1475del NP_001280124.1:p.Cys489LysfsTer11
NM_001293196.1:c.1189_1199del NP_001280125.1:p.Cys397LysfsTer11
NM_012222.2:c.1540_1550del NP_036354.1:p.Cys514LysfsTer11
XM_011541497.1:c.1525_1535del XP_011539799.1:p.Cys509LysfsTer11
XM_011541498.1:c.1507_1517del XP_011539800.1:p.Cys503LysfsTer11
XM_011541499.1:c.1507_1517del XP_011539801.1:p.Cys503LysfsTer11
XM_011541500.1:c.1507_1517del XP_011539802.1:p.Cys503LysfsTer11
XM_011541501.1:c.1507_1517del XP_011539803.1:p.Cys503LysfsTer11
XM_011541502.1:c.1507_1517del XP_011539804.1:p.Cys503LysfsTer11
XM_011541503.1:c.1507_1517del XP_011539805.1:p.Cys503LysfsTer11
XM_011541504.1:c.1498_1508del XP_011539806.1:p.Cys500LysfsTer11
XM_011541505.1:c.1087_1097del XP_011539807.1:p.Cys363LysfsTer11
XM_011541506.1:c.1087_1097del XP_011539808.1:p.Cys363LysfsTer11
XM_011541507.1:c.1078_1088del XP_011539809.1:p.Cys360LysfsTer11
XM_011541508.1:c.1093_1103del XP_011539810.1:p.Cys365LysfsTer11
XR_946658.1:n.1776_1786del
NM_001350650.1:c.1120_1130del NP_001337579.1:p.Cys374LysfsTer11
NM_001350651.1:c.1120_1130del NP_001337580.1:p.Cys374LysfsTer11
NR_146882.1:n.1903_1913del
NR_146883.1:n.1717_1727del
XM_011541497.3:c.1525_1535del XP_011539799.1:p.Cys509LysfsTer11
XM_011541500.3:c.1507_1517del XP_011539802.1:p.Cys503LysfsTer11
XM_011541501.2:c.1507_1517del XP_011539803.1:p.Cys503LysfsTer11
XM_011541502.2:c.1507_1517del XP_011539804.1:p.Cys503LysfsTer11
XM_011541503.2:c.1507_1517del XP_011539805.1:p.Cys503LysfsTer11
XM_011541504.2:c.1498_1508del XP_011539806.1:p.Cys500LysfsTer11
XM_011541505.2:c.1087_1097del XP_011539807.1:p.Cys363LysfsTer11
XM_011541506.2:c.1087_1097del XP_011539808.1:p.Cys363LysfsTer11
XM_017001331.1:c.1507_1517del XP_016856820.1:p.Cys503LysfsTer11
XM_017001332.1:c.1507_1517del XP_016856821.1:p.Cys503LysfsTer11
XM_017001333.1:c.1507_1517del XP_016856822.1:p.Cys503LysfsTer11
XM_017001334.1:c.1468_1478del XP_016856823.1:p.Cys490LysfsTer11
XM_017001335.1:c.1189_1199del XP_016856824.1:p.Cys397LysfsTer11
XM_017001336.1:c.1120_1130del XP_016856825.1:p.Cys374LysfsTer11
XM_017001337.1:c.1120_1130del XP_016856826.1:p.Cys374LysfsTer11
XM_024447244.1:c.1120_1130del XP_024303012.1:p.Cys374LysfsTer11
XM_024447245.1:c.1120_1130del XP_024303013.1:p.Cys374LysfsTer11
XM_024447248.1:c.1078_1088del XP_024303016.1:p.Cys360LysfsTer11
XM_024447249.1:c.949_959del XP_024303017.1:p.Cys317LysfsTer11
XM_024447250.1:c.949_959del XP_024303018.1:p.Cys317LysfsTer11
XM_024447251.1:c.949_959del XP_024303019.1:p.Cys317LysfsTer11
XR_001737190.1:n.1690_1700del
XR_001737192.1:n.1502_1512del
XR_002956643.1:n.1682_1692del
XR_002956644.1:n.2217_2227del
XR_946658.2:n.1790_1800del
NM_001048171.2:c.1465_1475del NP_001041636.2:p.Cys489LysfsTer11
NM_001128425.2:c.1549_1559del MANE Plus Clinical NP_001121897.1:p.Cys517LysfsTer11
NM_001048172.2:c.1468_1478del NP_001041637.1:p.Cys490LysfsTer11
NM_001048173.2:c.1465_1475del NP_001041638.1:p.Cys489LysfsTer11
NM_001048174.2:c.1465_1475del MANE Select NP_001041639.1:p.Cys489LysfsTer11
NM_001293190.2:c.1510_1520del NP_001280119.1:p.Cys504LysfsTer11
NM_001293191.2:c.1498_1508del NP_001280120.1:p.Cys500LysfsTer11
NM_001293192.2:c.1189_1199del NP_001280121.1:p.Cys397LysfsTer11
NM_001293195.2:c.1465_1475del NP_001280124.1:p.Cys489LysfsTer11
NM_001293196.2:c.1189_1199del NP_001280125.1:p.Cys397LysfsTer11
NM_001350650.2:c.1120_1130del NP_001337579.1:p.Cys374LysfsTer11
NM_001350651.2:c.1120_1130del NP_001337580.1:p.Cys374LysfsTer11
NM_012222.3:c.1540_1550del NP_036354.1:p.Cys514LysfsTer11
NR_146882.2:n.1873_1883del
NR_146883.2:n.1722_1732del