Canonical Allele Identifier: CA2495872559
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47475227_47475229delinsCGT , CM000664.2:g.47475227_47475229delinsCGT GRCh38
NC_000002.11:g.47702366_47702368delinsCGT , CM000664.1:g.47702366_47702368delinsCGT GRCh37
NC_000002.10:g.47555870_47555872delinsCGT NCBI36
NG_007110.2:g.77104_77106delinsCGT , LRG_218:g.77104_77106delinsCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.1962_1964delinsCGT ENSP00000495641.2:p.Asp654=
ENST00000233146.7:c.1962_1964delinsCGT MANE Select ENSP00000233146.2:p.Asp654=
ENST00000543555.6:c.1764_1766delinsCGT ENSP00000442697.1:p.Asp588=
ENST00000644092.1:c.*262_*264delinsCGT ENSP00000496351.1:n.*262_*264delinsCGT
ENST00000645339.1:c.1962_1964delinsCGT ENSP00000496441.1:p.Asp654=
ENST00000645506.1:c.1962_1964delinsCGT ENSP00000495455.1:p.Asp654=
ENST00000646415.1:c.1962_1964delinsCGT ENSP00000495543.1:p.Asp654=
ENST00000233146.6:c.1962_1964delinsCGT ENSP00000233146.2:p.Asp654=
ENST00000406134.5:c.1962_1964delinsCGT ENSP00000384199.1:p.Asp654=
ENST00000543555.5:c.1764_1766delinsCGT ENSP00000442697.1:p.Asp588=
ENST00000610696.4:c.*358_*360delinsCGT ENSP00000483159.1:n.*358_*360delinsCGT
ENST00000613514.4:c.*502_*504delinsCGT ENSP00000484137.1:n.*502_*504delinsCGT
ENST00000617333.3:c.*728_*730delinsCGT ENSP00000482468.1:n.*728_*730delinsCGT
ENST00000617938.4:c.*934_*936delinsCGT ENSP00000481158.1:n.*934_*936delinsCGT
ENST00000621359.2:c.1962_1964delinsCGT ENSP00000481416.1:p.Asp654=
NM_000251.2:c.1962_1964delinsCGT , LRG_218t1:c.1962_1964delinsCGT NP_000242.1:p.Asp654=
NM_001258281.1:c.1764_1766delinsCGT NP_001245210.1:p.Asp588=
XM_005264332.2:c.1962_1964delinsCGT XP_005264389.2:p.Asp654=
XM_011532867.1:c.1962_1964delinsCGT XP_011531169.1:p.Asp654=
XR_939685.1:n.2034_2036delinsCGT
XM_005264332.4:c.1962_1964delinsCGT XP_005264389.2:p.Asp654=
XM_011532867.2:c.1962_1964delinsCGT XP_011531169.1:p.Asp654=
XR_001738747.2:n.2024_2026delinsCGT
XR_939685.2:n.2024_2026delinsCGT
NM_000251.3:c.1962_1964delinsCGT MANE Select NP_000242.1:p.Asp654=