Canonical Allele Identifier: CA2586964825
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47475093_47475099delinsGA , CM000664.2:g.47475093_47475099delinsGA GRCh38
NC_000002.11:g.47702232_47702238delinsGA , CM000664.1:g.47702232_47702238delinsGA GRCh37
NC_000002.10:g.47555736_47555742delinsGA NCBI36
NG_007110.2:g.76970_76976delinsGA , LRG_218:g.76970_76976delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.1828_1834delinsGA ENSP00000495641.2:p.His610AspfsTer?
ENST00000233146.7:c.1828_1834delinsGA MANE Select ENSP00000233146.2:p.His610AspfsTer?
ENST00000543555.6:c.1630_1636delinsGA ENSP00000442697.1:p.His544AspfsTer?
ENST00000644092.1:c.*128_*134delinsGA ENSP00000496351.1:n.*128_*134delinsGA
ENST00000645339.1:c.1828_1834delinsGA ENSP00000496441.1:p.His610AspfsTer?
ENST00000645506.1:c.1828_1834delinsGA ENSP00000495455.1:p.His610AspfsTer?
ENST00000646415.1:c.1828_1834delinsGA ENSP00000495543.1:p.His610AspfsTer?
ENST00000233146.6:c.1828_1834delinsGA ENSP00000233146.2:p.His610AspfsTer?
ENST00000406134.5:c.1828_1834delinsGA ENSP00000384199.1:p.His610AspfsTer?
ENST00000543555.5:c.1630_1636delinsGA ENSP00000442697.1:p.His544AspfsTer?
ENST00000610696.4:c.*224_*230delinsGA ENSP00000483159.1:n.*224_*230delinsGA
ENST00000613514.4:c.*368_*374delinsGA ENSP00000484137.1:n.*368_*374delinsGA
ENST00000617333.3:c.*594_*600delinsGA ENSP00000482468.1:n.*594_*600delinsGA
ENST00000617938.4:c.*800_*806delinsGA ENSP00000481158.1:n.*800_*806delinsGA
ENST00000621359.2:c.1828_1834delinsGA ENSP00000481416.1:p.His610AspfsTer?
NM_000251.2:c.1828_1834delinsGA , LRG_218t1:c.1828_1834delinsGA NP_000242.1:p.His610AspfsTer?
NM_001258281.1:c.1630_1636delinsGA NP_001245210.1:p.His544AspfsTer?
XM_005264332.2:c.1828_1834delinsGA XP_005264389.2:p.His610AspfsTer?
XM_011532867.1:c.1828_1834delinsGA XP_011531169.1:p.His610AspfsTer?
XR_939685.1:n.1900_1906delinsGA
XM_005264332.4:c.1828_1834delinsGA XP_005264389.2:p.His610AspfsTer?
XM_011532867.2:c.1828_1834delinsGA XP_011531169.1:p.His610AspfsTer?
XR_001738747.2:n.1890_1896delinsGA
XR_939685.2:n.1890_1896delinsGA
NM_000251.3:c.1828_1834delinsGA MANE Select NP_000242.1:p.His610AspfsTer?