Canonical Allele Identifier: CA2473711271
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 998147
ClinVar RCV Id: RCV001293835
dbSNP Id: rs1644340673

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329310del , CM000663.2:g.45329310del GRCh38
NC_000001.10:g.45794982del , CM000663.1:g.45794982del GRCh37
NC_000001.9:g.45567569del NCBI36
NG_008189.1:g.16161del , LRG_220:g.16161del

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.1178del ENSP00000410263.2:p.Gln393ArgfsTer22
ENST00000435155.2:c.1595del ENSP00000403655.2:p.Gln532ArgfsTer?
ENST00000467459.6:c.*424del ENSP00000435889.2:n.*424del
ENST00000483127.2:c.1580del ENSP00000436469.2:p.Gln527ArgfsTer22
ENST00000485271.6:c.*305del ENSP00000431264.2:n.*305del
ENST00000529892.6:c.1415del ENSP00000432528.2:p.Gln472ArgfsTer?
ENST00000533178.6:c.*891del ENSP00000436430.2:n.*891del
ENST00000672314.2:c.1562del ENSP00000500828.2:p.Gln521ArgfsTer?
ENST00000710952.2:c.1646del MANE Plus Clinical ENSP00000518552.2:p.Gln549ArgfsTer22
ENST00000672818.3:c.1637del ENSP00000500891.1:p.Gln546ArgfsTer22
ENST00000456914.7:c.1562del MANE Select ENSP00000407590.2:p.Gln521ArgfsTer22
ENST00000671898.1:c.*305del ENSP00000499896.1:n.*305del
ENST00000672011.1:c.*891del ENSP00000500418.1:n.*891del
ENST00000672818.2:c.1637del ENSP00000500891.1:p.Gln546ArgfsTer22
ENST00000354383.10:c.1565del ENSP00000346354.6:p.Gln522ArgfsTer22
ENST00000355498.6:c.1562del ENSP00000347685.2:p.Gln521ArgfsTer22
ENST00000372098.7:c.1637del ENSP00000361170.3:p.Gln546ArgfsTer22
ENST00000372104.5:c.1562del ENSP00000361176.1:p.Gln521ArgfsTer22
ENST00000372110.7:c.1607del ENSP00000361182.3:p.Gln536ArgfsTer22
ENST00000372115.7:c.1604del ENSP00000361187.3:p.Gln535ArgfsTer22
ENST00000448481.5:c.1595del ENSP00000409718.1:p.Gln532ArgfsTer22
ENST00000450313.5:c.1646del ENSP00000408176.1:p.Gln549ArgfsTer22
ENST00000456914.6:c.1562del ENSP00000407590.2:p.Gln521ArgfsTer22
ENST00000467459.5:c.979del ENSP00000435889.1:n.979del
ENST00000475516.5:c.*1375del ENSP00000433843.1:n.*1375del
ENST00000481571.5:c.*1375del ENSP00000436597.1:n.*1375del
ENST00000482094.5:n.883del
ENST00000485271.5:c.439del
ENST00000488731.6:c.647del ENSP00000432330.1:p.Gln216ArgfsTer22
ENST00000528013.6:c.1604del ENSP00000433130.2:p.Gln535ArgfsTer?
ENST00000529892.5:c.637del
ENST00000529984.5:c.647del ENSP00000437093.1:p.Gln216ArgfsTer22
ENST00000531105.5:c.*54del ENSP00000431292.1:n.*54del
ENST00000533178.5:c.1191del ENSP00000436430.1:n.1191del
NM_001048171.1:c.1604del NP_001041636.1:p.Gln535ArgfsTer22
NM_001048172.1:c.1565del NP_001041637.1:p.Gln522ArgfsTer22
NM_001048173.1:c.1562del NP_001041638.1:p.Gln521ArgfsTer22
NM_001048174.1:c.1562del NP_001041639.1:p.Gln521ArgfsTer22
NM_001128425.1:c.1646del , LRG_220t1:c.1646del NP_001121897.1:p.Gln549ArgfsTer22
NM_001293190.1:c.1607del NP_001280119.1:p.Gln536ArgfsTer22
NM_001293191.1:c.1595del NP_001280120.1:p.Gln532ArgfsTer22
NM_001293192.1:c.1286del NP_001280121.1:p.Gln429ArgfsTer22
NM_001293195.1:c.1562del NP_001280124.1:p.Gln521ArgfsTer22
NM_001293196.1:c.1286del NP_001280125.1:p.Gln429ArgfsTer22
NM_012222.2:c.1637del NP_036354.1:p.Gln546ArgfsTer22
XM_011541497.1:c.1622del XP_011539799.1:p.Gln541ArgfsTer22
XM_011541498.1:c.1604del XP_011539800.1:p.Gln535ArgfsTer22
XM_011541499.1:c.1604del XP_011539801.1:p.Gln535ArgfsTer22
XM_011541500.1:c.1604del XP_011539802.1:p.Gln535ArgfsTer22
XM_011541501.1:c.1604del XP_011539803.1:p.Gln535ArgfsTer22
XM_011541502.1:c.1604del XP_011539804.1:p.Gln535ArgfsTer22
XM_011541503.1:c.1604del XP_011539805.1:p.Gln535ArgfsTer22
XM_011541504.1:c.1595del XP_011539806.1:p.Gln532ArgfsTer22
XM_011541505.1:c.1184del XP_011539807.1:p.Gln395ArgfsTer22
XM_011541506.1:c.1184del XP_011539808.1:p.Gln395ArgfsTer22
XM_011541507.1:c.1175del XP_011539809.1:p.Gln392ArgfsTer22
XM_011541508.1:c.1190del XP_011539810.1:p.Gln397ArgfsTer22
XR_946658.1:n.1873del
NM_001350650.1:c.1217del NP_001337579.1:p.Gln406ArgfsTer22
NM_001350651.1:c.1217del NP_001337580.1:p.Gln406ArgfsTer22
NR_146882.1:n.2000del
NR_146883.1:n.1814del
XM_011541497.3:c.1622del XP_011539799.1:p.Gln541ArgfsTer22
XM_011541500.3:c.1604del XP_011539802.1:p.Gln535ArgfsTer22
XM_011541501.2:c.1604del XP_011539803.1:p.Gln535ArgfsTer22
XM_011541502.2:c.1604del XP_011539804.1:p.Gln535ArgfsTer22
XM_011541503.2:c.1604del XP_011539805.1:p.Gln535ArgfsTer22
XM_011541504.2:c.1595del XP_011539806.1:p.Gln532ArgfsTer22
XM_011541505.2:c.1184del XP_011539807.1:p.Gln395ArgfsTer22
XM_011541506.2:c.1184del XP_011539808.1:p.Gln395ArgfsTer22
XM_017001331.1:c.1604del XP_016856820.1:p.Gln535ArgfsTer22
XM_017001332.1:c.1604del XP_016856821.1:p.Gln535ArgfsTer22
XM_017001333.1:c.1604del XP_016856822.1:p.Gln535ArgfsTer22
XM_017001334.1:c.1565del XP_016856823.1:p.Gln522ArgfsTer22
XM_017001335.1:c.1286del XP_016856824.1:p.Gln429ArgfsTer22
XM_017001336.1:c.1217del XP_016856825.1:p.Gln406ArgfsTer22
XM_017001337.1:c.1217del XP_016856826.1:p.Gln406ArgfsTer22
XM_024447244.1:c.1217del XP_024303012.1:p.Gln406ArgfsTer22
XM_024447245.1:c.1217del XP_024303013.1:p.Gln406ArgfsTer22
XM_024447248.1:c.1175del XP_024303016.1:p.Gln392ArgfsTer22
XM_024447249.1:c.1046del XP_024303017.1:p.Gln349ArgfsTer22
XM_024447250.1:c.1046del XP_024303018.1:p.Gln349ArgfsTer22
XM_024447251.1:c.1046del XP_024303019.1:p.Gln349ArgfsTer22
XR_001737190.1:n.1787del
XR_001737192.1:n.1599del
XR_002956643.1:n.1779del
XR_002956644.1:n.2314del
XR_946658.2:n.1887del
NM_001048171.2:c.1562del NP_001041636.2:p.Gln521ArgfsTer22
NM_001128425.2:c.1646del MANE Plus Clinical NP_001121897.1:p.Gln549ArgfsTer22
NM_001048172.2:c.1565del NP_001041637.1:p.Gln522ArgfsTer22
NM_001048173.2:c.1562del NP_001041638.1:p.Gln521ArgfsTer22
NM_001048174.2:c.1562del MANE Select NP_001041639.1:p.Gln521ArgfsTer22
NM_001293190.2:c.1607del NP_001280119.1:p.Gln536ArgfsTer22
NM_001293191.2:c.1595del NP_001280120.1:p.Gln532ArgfsTer22
NM_001293192.2:c.1286del NP_001280121.1:p.Gln429ArgfsTer22
NM_001293195.2:c.1562del NP_001280124.1:p.Gln521ArgfsTer22
NM_001293196.2:c.1286del NP_001280125.1:p.Gln429ArgfsTer22
NM_001350650.2:c.1217del NP_001337579.1:p.Gln406ArgfsTer22
NM_001350651.2:c.1217del NP_001337580.1:p.Gln406ArgfsTer22
NM_012222.3:c.1637del NP_036354.1:p.Gln546ArgfsTer22
NR_146882.2:n.1970del
NR_146883.2:n.1819del