Canonical Allele Identifier: CA346797
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182684
dbSNP Id: rs864621967

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331177_45331183del , CM000663.2:g.45331177_45331183del GRCh38
NC_000001.10:g.45796849_45796855del , CM000663.1:g.45796849_45796855del GRCh37
NC_000001.9:g.45569436_45569442del NCBI36
NG_008189.1:g.14289_14295del , LRG_220:g.14289_14295del

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.1008_1008+6del
ENST00000435155.2:c.1425_1425+6del
ENST00000467459.6:c.*254_*254+6del
ENST00000483127.2:c.1410_1410+6del
ENST00000485271.6:c.1392_1392+6del
ENST00000529892.6:c.1245_1245+6del
ENST00000533178.6:c.*721_*721+6del
ENST00000672314.2:c.1392_1392+6del
ENST00000710952.2:c.1476_1476+6del
ENST00000672818.3:c.1467_1467+6del
ENST00000456914.7:c.1392_1392+6del
ENST00000671898.1:c.1980_1980+6del
ENST00000672011.1:c.*721_*721+6del
ENST00000672314.1:c.1392_1392+6del
ENST00000672818.2:c.1467_1467+6del
ENST00000673134.1:c.*1089_*1089+6del
ENST00000354383.10:c.1395_1395+6del
ENST00000355498.6:c.1392_1392+6del
ENST00000372098.7:c.1467_1467+6del
ENST00000372104.5:c.1392_1392+6del
ENST00000372110.7:c.1437_1437+6del
ENST00000372115.7:c.1434_1434+6del
ENST00000448481.5:c.1425_1425+6del
ENST00000450313.5:c.1476_1476+6del
ENST00000456914.6:c.1392_1392+6del
ENST00000467459.5:c.809_809+6del
ENST00000475516.5:c.*1205_*1205+6del
ENST00000481571.5:c.*1205_*1205+6del
ENST00000482094.5:n.713_713+6del
ENST00000485271.5:c.89_89+6del
ENST00000488731.6:c.477_477+6del
ENST00000528013.6:c.1434_1434+6del
ENST00000529892.5:c.467_467+6del
ENST00000529984.5:c.477_477+6del
ENST00000531105.5:c.116-1745_116-1739del ENSP00000431292.1:n.116-1745_116-1739del
ENST00000533178.5:c.1021_1021+6del
NM_001048171.1:c.1434_1434+6del
NM_001048172.1:c.1395_1395+6del
NM_001048173.1:c.1392_1392+6del
NM_001048174.1:c.1392_1392+6del
NM_001128425.1:c.1476_1476+6del , LRG_220t1:c.1476_1476+6del
NM_001293190.1:c.1437_1437+6del
NM_001293191.1:c.1425_1425+6del
NM_001293192.1:c.1116_1116+6del
NM_001293195.1:c.1392_1392+6del
NM_001293196.1:c.1116_1116+6del
NM_012222.2:c.1467_1467+6del
XM_011541497.1:c.1452_1452+6del
XM_011541498.1:c.1434_1434+6del
XM_011541499.1:c.1434_1434+6del
XM_011541500.1:c.1434_1434+6del
XM_011541501.1:c.1434_1434+6del
XM_011541502.1:c.1434_1434+6del
XM_011541503.1:c.1434_1434+6del
XM_011541504.1:c.1425_1425+6del
XM_011541505.1:c.1014_1014+6del
XM_011541506.1:c.1014_1014+6del
XM_011541507.1:c.1005_1005+6del
XM_011541508.1:c.1020_1020+6del
XR_946658.1:n.1523_1523+6del
NM_001350650.1:c.1047_1047+6del
NM_001350651.1:c.1047_1047+6del
NR_146882.1:n.1650_1650+6del
NR_146883.1:n.1464_1464+6del
XM_011541497.3:c.1452_1452+6del
XM_011541500.3:c.1434_1434+6del
XM_011541501.2:c.1434_1434+6del
XM_011541502.2:c.1434_1434+6del
XM_011541503.2:c.1434_1434+6del
XM_011541504.2:c.1425_1425+6del
XM_011541505.2:c.1014_1014+6del
XM_011541506.2:c.1014_1014+6del
XM_017001331.1:c.1434_1434+6del
XM_017001332.1:c.1434_1434+6del
XM_017001333.1:c.1434_1434+6del
XM_017001334.1:c.1395_1395+6del
XM_017001335.1:c.1116_1116+6del
XM_017001336.1:c.1047_1047+6del
XM_017001337.1:c.1047_1047+6del
XM_024447244.1:c.1047_1047+6del
XM_024447245.1:c.1047_1047+6del
XM_024447248.1:c.1005_1005+6del
XM_024447249.1:c.876_876+6del
XM_024447250.1:c.876_876+6del
XM_024447251.1:c.876_876+6del
XR_001737190.1:n.1437_1437+6del
XR_001737192.1:n.1249_1249+6del
XR_002956643.1:n.1429_1429+6del
XR_002956644.1:n.1964_1964+6del
XR_946658.2:n.1537_1537+6del
NM_001048171.2:c.1392_1392+6del
NM_001128425.2:c.1476_1476+6del
NM_001048172.2:c.1395_1395+6del
NM_001048173.2:c.1392_1392+6del
NM_001048174.2:c.1392_1392+6del
NM_001293190.2:c.1437_1437+6del
NM_001293191.2:c.1425_1425+6del
NM_001293192.2:c.1116_1116+6del
NM_001293195.2:c.1392_1392+6del
NM_001293196.2:c.1116_1116+6del
NM_001350650.2:c.1047_1047+6del
NM_001350651.2:c.1047_1047+6del
NM_012222.3:c.1467_1467+6del
NR_146882.2:n.1620_1620+6del
NR_146883.2:n.1469_1469+6del