Canonical Allele Identifier: CA522810435
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1490948
ClinVar RCV Id: RCV001986174
dbSNP Id: rs1557472384

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332325_45332405del , CM000663.2:g.45332325_45332405del GRCh38
NC_000001.10:g.45797997_45798077del , CM000663.1:g.45797997_45798077del GRCh37
NC_000001.9:g.45570584_45570664del NCBI36
NG_008189.1:g.13071_13151del , LRG_220:g.13071_13151del

Transcript Alleles

HGVS Amino-acid change
ENST00000672818.3:c.770_780-10del
ENST00000450313.6:c.*24_*34-10del
ENST00000456914.7:c.695_705-10del
ENST00000461495.6:c.*434_*444-10del
ENST00000671898.1:c.1283_1293-10del
ENST00000672011.1:c.*24_*34-10del
ENST00000672314.1:c.695_705-10del
ENST00000672593.1:c.*668_*748del ENSP00000500455.1:n.*668_*748del
ENST00000672764.1:c.*24_*34-10del
ENST00000672818.2:c.770_780-10del
ENST00000673134.1:c.*392_*402-10del
ENST00000674679.1:n.723_733-10del
ENST00000354383.10:c.698_708-10del
ENST00000355498.6:c.695_705-10del
ENST00000372098.7:c.770_780-10del
ENST00000372104.5:c.695_705-10del
ENST00000372110.7:c.740_750-10del
ENST00000372115.7:c.737_747-10del
ENST00000412971.5:c.311_321-10del
ENST00000435155.1:c.728_738-10del
ENST00000448481.5:c.728_738-10del
ENST00000450313.5:c.779_789-10del
ENST00000456914.6:c.695_705-10del
ENST00000461495.5:c.*434_*444-10del
ENST00000462388.5:n.386_396-10del
ENST00000467459.5:n.89_99-10del
ENST00000467940.5:c.*618_*628-10del
ENST00000470256.5:c.*24_*34-10del
ENST00000475516.5:c.*508_*518-10del
ENST00000478796.5:n.682_692-10del
ENST00000481571.5:c.*508_*518-10del
ENST00000488731.6:c.187+363_187+443del ENSP00000432330.1:n.187+363_187+443del
ENST00000528013.6:c.737_747-10del
ENST00000529984.5:c.187+363_187+443del ENSP00000437093.1:n.187+363_187+443del
ENST00000531105.5:c.115+1991_115+2071del ENSP00000431292.1:n.115+1991_115+2071del
ENST00000533178.5:n.324_334-10del
NM_001048171.1:c.737_747-10del
NM_001048172.1:c.698_708-10del
NM_001048173.1:c.695_705-10del
NM_001048174.1:c.695_705-10del
NM_001128425.1:c.779_789-10del , LRG_220t1:c.779_789-10del
NM_001293190.1:c.740_750-10del
NM_001293191.1:c.728_738-10del
NM_001293192.1:c.419_429-10del
NM_001293195.1:c.695_705-10del
NM_001293196.1:c.419_429-10del
NM_012222.2:c.770_780-10del
XM_011541497.1:c.755_765-10del
XM_011541498.1:c.737_747-10del
XM_011541499.1:c.737_747-10del
XM_011541500.1:c.737_747-10del
XM_011541501.1:c.737_747-10del
XM_011541502.1:c.737_747-10del
XM_011541503.1:c.737_747-10del
XM_011541504.1:c.728_738-10del
XM_011541505.1:c.317_327-10del
XM_011541506.1:c.317_327-10del
XM_011541507.1:c.308_318-10del
XM_011541508.1:c.323_333-10del
XR_946658.1:n.826_836-10del
NM_001350650.1:c.350_360-10del
NM_001350651.1:c.350_360-10del
NR_146882.1:n.953_963-10del
NR_146883.1:n.767_777-10del
XM_011541497.3:c.755_765-10del
XM_011541500.3:c.737_747-10del
XM_011541501.2:c.737_747-10del
XM_011541502.2:c.737_747-10del
XM_011541503.2:c.737_747-10del
XM_011541504.2:c.728_738-10del
XM_011541505.2:c.317_327-10del
XM_011541506.2:c.317_327-10del
XM_017001331.1:c.737_747-10del
XM_017001332.1:c.737_747-10del
XM_017001333.1:c.737_747-10del
XM_017001334.1:c.698_708-10del
XM_017001335.1:c.419_429-10del
XM_017001336.1:c.350_360-10del
XM_017001337.1:c.350_360-10del
XM_024447244.1:c.350_360-10del
XM_024447245.1:c.350_360-10del
XM_024447248.1:c.308_318-10del
XM_024447249.1:c.179_189-10del
XM_024447250.1:c.179_189-10del
XM_024447251.1:c.179_189-10del
XR_001737190.1:n.740_750-10del
XR_001737192.1:n.552_562-10del
XR_002956643.1:n.732_742-10del
XR_002956644.1:n.1267_1277-10del
XR_946658.2:n.840_850-10del
NM_001048171.2:c.695_705-10del
NM_001128425.2:c.779_789-10del
NM_001048172.2:c.698_708-10del
NM_001048173.2:c.695_705-10del
NM_001048174.2:c.695_705-10del
NM_001293190.2:c.740_750-10del
NM_001293191.2:c.728_738-10del
NM_001293192.2:c.419_429-10del
NM_001293195.2:c.695_705-10del
NM_001293196.2:c.419_429-10del
NM_001350650.2:c.350_360-10del
NM_001350651.2:c.350_360-10del
NM_012222.3:c.770_780-10del
NR_146882.2:n.923_933-10del
NR_146883.2:n.772_782-10del