Canonical Allele Identifier: CA2499214751
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1050536
ClinVar RCV Id: RCV001358085

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329304_45330608del , CM000663.2:g.45329304_45330608del GRCh38
NC_000001.10:g.45794976_45796280del , CM000663.1:g.45794976_45796280del GRCh37
NC_000001.9:g.45567563_45568867del NCBI36
NG_008189.1:g.14863_16167del , LRG_220:g.14863_16167del

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.1009-51_*2del
ENST00000435155.2:c.1426-51_*2del
ENST00000467459.6:c.*255-51_*430del
ENST00000483127.2:c.1411-51_*2del
ENST00000485271.6:c.1393-51_*311del
ENST00000529892.6:c.1246-51_*2del
ENST00000533178.6:c.*722-51_*897del
ENST00000672314.2:c.1393-51_*2del
ENST00000710952.2:c.1477-51_*2del
ENST00000672818.3:c.1468-51_*2del
ENST00000456914.7:c.1393-51_*2del
ENST00000671898.1:c.1981-51_*311del
ENST00000672011.1:c.*722-51_*897del
ENST00000672818.2:c.1468-51_*2del
ENST00000354383.10:c.1396-51_*2del
ENST00000355498.6:c.1393-51_*2del
ENST00000372098.7:c.1468-51_*2del
ENST00000372104.5:c.1393-51_*2del
ENST00000372110.7:c.1438-51_*2del
ENST00000372115.7:c.1435-51_*2del
ENST00000448481.5:c.1426-51_*2del
ENST00000450313.5:c.1477-51_*2del
ENST00000456914.6:c.1393-51_*2del
ENST00000467459.5:c.810-51_985del
ENST00000475516.5:c.*1206-51_*1381del
ENST00000481571.5:c.*1206-51_*1381del
ENST00000482094.5:n.714-51_889del
ENST00000485271.5:c.90-51_445del
ENST00000488731.6:c.478-51_*2del
ENST00000529892.5:c.468-51_643del
ENST00000529984.5:c.478-51_*2del
ENST00000531105.5:c.116-1171_*60del
ENST00000533178.5:c.1022-51_1197del
NM_001048171.1:c.1435-51_*2del
NM_001048172.1:c.1396-51_*2del
NM_001048173.1:c.1393-51_*2del
NM_001048174.1:c.1393-51_*2del
NM_001128425.1:c.1477-51_*2del , LRG_220t1:c.1477-51_*2del
NM_001293190.1:c.1438-51_*2del
NM_001293191.1:c.1426-51_*2del
NM_001293192.1:c.1117-51_*2del
NM_001293195.1:c.1393-51_*2del
NM_001293196.1:c.1117-51_*2del
NM_012222.2:c.1468-51_*2del
XM_011541497.1:c.1453-51_*2del
XM_011541498.1:c.1435-51_*2del
XM_011541499.1:c.1435-51_*2del
XM_011541500.1:c.1435-51_*2del
XM_011541501.1:c.1435-51_*2del
XM_011541502.1:c.1435-51_*2del
XM_011541503.1:c.1435-51_*2del
XM_011541504.1:c.1426-51_*2del
XM_011541505.1:c.1015-51_*2del
XM_011541506.1:c.1015-51_*2del
XM_011541507.1:c.1006-51_*2del
XM_011541508.1:c.1021-51_*2del
XR_946658.1:n.1524-51_1879del
NM_001350650.1:c.1048-51_*2del
NM_001350651.1:c.1048-51_*2del
NR_146882.1:n.1651-51_2006del
NR_146883.1:n.1465-51_1820del
XM_011541497.3:c.1453-51_*2del
XM_011541500.3:c.1435-51_*2del
XM_011541501.2:c.1435-51_*2del
XM_011541502.2:c.1435-51_*2del
XM_011541503.2:c.1435-51_*2del
XM_011541504.2:c.1426-51_*2del
XM_011541505.2:c.1015-51_*2del
XM_011541506.2:c.1015-51_*2del
XM_017001331.1:c.1435-51_*2del
XM_017001332.1:c.1435-51_*2del
XM_017001333.1:c.1435-51_*2del
XM_017001334.1:c.1396-51_*2del
XM_017001335.1:c.1117-51_*2del
XM_017001336.1:c.1048-51_*2del
XM_017001337.1:c.1048-51_*2del
XM_024447244.1:c.1048-51_*2del
XM_024447245.1:c.1048-51_*2del
XM_024447248.1:c.1006-51_*2del
XM_024447249.1:c.877-51_*2del
XM_024447250.1:c.877-51_*2del
XM_024447251.1:c.877-51_*2del
XR_001737190.1:n.1438-51_1793del
XR_001737192.1:n.1250-51_1605del
XR_002956643.1:n.1430-51_1785del
XR_002956644.1:n.1965-51_2320del
XR_946658.2:n.1538-51_1893del
NM_001048171.2:c.1393-51_*2del
NM_001128425.2:c.1477-51_*2del
NM_001048172.2:c.1396-51_*2del
NM_001048173.2:c.1393-51_*2del
NM_001048174.2:c.1393-51_*2del
NM_001293190.2:c.1438-51_*2del
NM_001293191.2:c.1426-51_*2del
NM_001293192.2:c.1117-51_*2del
NM_001293195.2:c.1393-51_*2del
NM_001293196.2:c.1117-51_*2del
NM_001350650.2:c.1048-51_*2del
NM_001350651.2:c.1048-51_*2del
NM_012222.3:c.1468-51_*2del
NR_146882.2:n.1621-51_1976del
NR_146883.2:n.1470-51_1825del