Canonical Allele Identifier: CA2739272327
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2834935
ClinVar RCV Id: RCV003613964

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329398_45329431del , CM000663.2:g.45329398_45329431del GRCh38
NC_000001.10:g.45795070_45795103del , CM000663.1:g.45795070_45795103del GRCh37
NC_000001.9:g.45567657_45567690del NCBI36
NG_008189.1:g.16045_16078del , LRG_220:g.16045_16078del

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.1062_1095del ENSP00000410263.2:p.Arg354SerfsTer?
ENST00000435155.2:c.1479_1512del ENSP00000403655.2:p.Arg493SerfsTer?
ENST00000467459.6:c.*308_*341del ENSP00000435889.2:n.*308_*341del
ENST00000483127.2:c.1464_1497del ENSP00000436469.2:p.Arg488SerfsTer?
ENST00000485271.6:c.*189_*222del ENSP00000431264.2:n.*189_*222del
ENST00000529892.6:c.1299_1332del ENSP00000432528.2:p.Arg433SerfsTer?
ENST00000533178.6:c.*775_*808del ENSP00000436430.2:n.*775_*808del
ENST00000672314.2:c.1446_1479del ENSP00000500828.2:p.Arg482SerfsTer?
ENST00000710952.2:c.1530_1563del MANE Plus Clinical ENSP00000518552.2:p.Arg510SerfsTer?
ENST00000672818.3:c.1521_1554del ENSP00000500891.1:p.Arg507SerfsTer?
ENST00000456914.7:c.1446_1479del MANE Select ENSP00000407590.2:p.Arg482SerfsTer?
ENST00000671898.1:c.*189_*222del ENSP00000499896.1:n.*189_*222del
ENST00000672011.1:c.*775_*808del ENSP00000500418.1:n.*775_*808del
ENST00000672818.2:c.1521_1554del ENSP00000500891.1:p.Arg507SerfsTer?
ENST00000354383.10:c.1449_1482del ENSP00000346354.6:p.Arg483SerfsTer?
ENST00000355498.6:c.1446_1479del ENSP00000347685.2:p.Arg482SerfsTer?
ENST00000372098.7:c.1521_1554del ENSP00000361170.3:p.Arg507SerfsTer?
ENST00000372104.5:c.1446_1479del ENSP00000361176.1:p.Arg482SerfsTer?
ENST00000372110.7:c.1491_1524del ENSP00000361182.3:p.Arg497SerfsTer?
ENST00000372115.7:c.1488_1521del ENSP00000361187.3:p.Arg496SerfsTer?
ENST00000448481.5:c.1479_1512del ENSP00000409718.1:p.Arg493SerfsTer?
ENST00000450313.5:c.1530_1563del ENSP00000408176.1:p.Arg510SerfsTer?
ENST00000456914.6:c.1446_1479del ENSP00000407590.2:p.Arg482SerfsTer?
ENST00000467459.5:c.863_896del ENSP00000435889.1:n.863_896del
ENST00000475516.5:c.*1259_*1292del ENSP00000433843.1:n.*1259_*1292del
ENST00000481571.5:c.*1259_*1292del ENSP00000436597.1:n.*1259_*1292del
ENST00000482094.5:n.767_800del
ENST00000485271.5:c.323_356del
ENST00000488731.6:c.531_564del ENSP00000432330.1:p.Arg177SerfsTer?
ENST00000528013.6:c.1488_1521del ENSP00000433130.2:p.Arg496SerfsTer?
ENST00000529892.5:c.521_554del
ENST00000529984.5:c.531_564del ENSP00000437093.1:p.Arg177SerfsTer?
ENST00000531105.5:c.127_160del ENSP00000431292.1:p.Val43ProfsTer29
ENST00000533178.5:c.1075_1108del ENSP00000436430.1:n.1075_1108del
NM_001048171.1:c.1488_1521del NP_001041636.1:p.Arg496SerfsTer?
NM_001048172.1:c.1449_1482del NP_001041637.1:p.Arg483SerfsTer?
NM_001048173.1:c.1446_1479del NP_001041638.1:p.Arg482SerfsTer?
NM_001048174.1:c.1446_1479del NP_001041639.1:p.Arg482SerfsTer?
NM_001128425.1:c.1530_1563del , LRG_220t1:c.1530_1563del NP_001121897.1:p.Arg510SerfsTer?
NM_001293190.1:c.1491_1524del NP_001280119.1:p.Arg497SerfsTer?
NM_001293191.1:c.1479_1512del NP_001280120.1:p.Arg493SerfsTer?
NM_001293192.1:c.1170_1203del NP_001280121.1:p.Arg390SerfsTer?
NM_001293195.1:c.1446_1479del NP_001280124.1:p.Arg482SerfsTer?
NM_001293196.1:c.1170_1203del NP_001280125.1:p.Arg390SerfsTer?
NM_012222.2:c.1521_1554del NP_036354.1:p.Arg507SerfsTer?
XM_011541497.1:c.1506_1539del XP_011539799.1:p.Arg502SerfsTer?
XM_011541498.1:c.1488_1521del XP_011539800.1:p.Arg496SerfsTer?
XM_011541499.1:c.1488_1521del XP_011539801.1:p.Arg496SerfsTer?
XM_011541500.1:c.1488_1521del XP_011539802.1:p.Arg496SerfsTer?
XM_011541501.1:c.1488_1521del XP_011539803.1:p.Arg496SerfsTer?
XM_011541502.1:c.1488_1521del XP_011539804.1:p.Arg496SerfsTer?
XM_011541503.1:c.1488_1521del XP_011539805.1:p.Arg496SerfsTer?
XM_011541504.1:c.1479_1512del XP_011539806.1:p.Arg493SerfsTer?
XM_011541505.1:c.1068_1101del XP_011539807.1:p.Arg356SerfsTer?
XM_011541506.1:c.1068_1101del XP_011539808.1:p.Arg356SerfsTer?
XM_011541507.1:c.1059_1092del XP_011539809.1:p.Arg353SerfsTer?
XM_011541508.1:c.1074_1107del XP_011539810.1:p.Arg358SerfsTer?
XR_946658.1:n.1757_1790del
NM_001350650.1:c.1101_1134del NP_001337579.1:p.Arg367SerfsTer?
NM_001350651.1:c.1101_1134del NP_001337580.1:p.Arg367SerfsTer?
NR_146882.1:n.1884_1917del
NR_146883.1:n.1698_1731del
XM_011541497.3:c.1506_1539del XP_011539799.1:p.Arg502SerfsTer?
XM_011541500.3:c.1488_1521del XP_011539802.1:p.Arg496SerfsTer?
XM_011541501.2:c.1488_1521del XP_011539803.1:p.Arg496SerfsTer?
XM_011541502.2:c.1488_1521del XP_011539804.1:p.Arg496SerfsTer?
XM_011541503.2:c.1488_1521del XP_011539805.1:p.Arg496SerfsTer?
XM_011541504.2:c.1479_1512del XP_011539806.1:p.Arg493SerfsTer?
XM_011541505.2:c.1068_1101del XP_011539807.1:p.Arg356SerfsTer?
XM_011541506.2:c.1068_1101del XP_011539808.1:p.Arg356SerfsTer?
XM_017001331.1:c.1488_1521del XP_016856820.1:p.Arg496SerfsTer?
XM_017001332.1:c.1488_1521del XP_016856821.1:p.Arg496SerfsTer?
XM_017001333.1:c.1488_1521del XP_016856822.1:p.Arg496SerfsTer?
XM_017001334.1:c.1449_1482del XP_016856823.1:p.Arg483SerfsTer?
XM_017001335.1:c.1170_1203del XP_016856824.1:p.Arg390SerfsTer?
XM_017001336.1:c.1101_1134del XP_016856825.1:p.Arg367SerfsTer?
XM_017001337.1:c.1101_1134del XP_016856826.1:p.Arg367SerfsTer?
XM_024447244.1:c.1101_1134del XP_024303012.1:p.Arg367SerfsTer?
XM_024447245.1:c.1101_1134del XP_024303013.1:p.Arg367SerfsTer?
XM_024447248.1:c.1059_1092del XP_024303016.1:p.Arg353SerfsTer?
XM_024447249.1:c.930_963del XP_024303017.1:p.Arg310SerfsTer?
XM_024447250.1:c.930_963del XP_024303018.1:p.Arg310SerfsTer?
XM_024447251.1:c.930_963del XP_024303019.1:p.Arg310SerfsTer?
XR_001737190.1:n.1671_1704del
XR_001737192.1:n.1483_1516del
XR_002956643.1:n.1663_1696del
XR_002956644.1:n.2198_2231del
XR_946658.2:n.1771_1804del
NM_001048171.2:c.1446_1479del NP_001041636.2:p.Arg482SerfsTer?
NM_001128425.2:c.1530_1563del MANE Plus Clinical NP_001121897.1:p.Arg510SerfsTer?
NM_001048172.2:c.1449_1482del NP_001041637.1:p.Arg483SerfsTer?
NM_001048173.2:c.1446_1479del NP_001041638.1:p.Arg482SerfsTer?
NM_001048174.2:c.1446_1479del MANE Select NP_001041639.1:p.Arg482SerfsTer?
NM_001293190.2:c.1491_1524del NP_001280119.1:p.Arg497SerfsTer?
NM_001293191.2:c.1479_1512del NP_001280120.1:p.Arg493SerfsTer?
NM_001293192.2:c.1170_1203del NP_001280121.1:p.Arg390SerfsTer?
NM_001293195.2:c.1446_1479del NP_001280124.1:p.Arg482SerfsTer?
NM_001293196.2:c.1170_1203del NP_001280125.1:p.Arg390SerfsTer?
NM_001350650.2:c.1101_1134del NP_001337579.1:p.Arg367SerfsTer?
NM_001350651.2:c.1101_1134del NP_001337580.1:p.Arg367SerfsTer?
NM_012222.3:c.1521_1554del NP_036354.1:p.Arg507SerfsTer?
NR_146882.2:n.1854_1887del
NR_146883.2:n.1703_1736del