Canonical Allele Identifier: CA16611064
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408472
dbSNP Id: rs1060501998
gnomAD v4: 2-47482878-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47482878A>C , CM000664.2:g.47482878A>C GRCh38
NC_000002.11:g.47710017A>C , CM000664.1:g.47710017A>C GRCh37
NC_000002.10:g.47563521A>C NCBI36
NG_007110.2:g.84755A>C , LRG_218:g.84755A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.2634+2007A>C ENSP00000495641.2:n.2634+2007A>C
ENST00000233146.7:c.2734A>C MANE Select ENSP00000233146.2:p.Lys912Gln
ENST00000543555.6:c.2536A>C ENSP00000442697.1:p.Lys846Gln
ENST00000644092.1:c.*934+2007A>C ENSP00000496351.1:n.*934+2007A>C
ENST00000644900.1:c.487+2007A>C
ENST00000645339.1:c.2634+2007A>C ENSP00000496441.1:n.2634+2007A>C
ENST00000645506.1:c.2634+2007A>C ENSP00000495455.1:n.2634+2007A>C
ENST00000646415.1:c.2634+2007A>C ENSP00000495543.1:n.2634+2007A>C
ENST00000233146.6:c.2734A>C ENSP00000233146.2:p.Lys912Gln
ENST00000406134.5:c.2634+2007A>C ENSP00000384199.1:n.2634+2007A>C
ENST00000461394.5:n.75+2007A>C
ENST00000543555.5:c.2536A>C ENSP00000442697.1:p.Lys846Gln
ENST00000610696.4:c.*1130A>C ENSP00000483159.1:n.*1130A>C
ENST00000613514.4:c.*1274A>C ENSP00000484137.1:n.*1274A>C
ENST00000617333.3:c.*1500A>C ENSP00000482468.1:n.*1500A>C
ENST00000617938.4:c.*1706A>C ENSP00000481158.1:n.*1706A>C
ENST00000621359.2:c.*300A>C ENSP00000481416.1:n.*300A>C
NM_000251.2:c.2734A>C , LRG_218t1:c.2734A>C NP_000242.1:p.Lys912Gln
NM_001258281.1:c.2536A>C NP_001245210.1:p.Lys846Gln
XM_005264332.2:c.2634+2007A>C XP_005264389.2:n.2634+2007A>C
XM_011532867.1:c.2634+2007A>C XP_011531169.1:n.2634+2007A>C
XR_939685.1:n.2706+2007A>C
XM_005264332.4:c.2634+2007A>C XP_005264389.2:n.2634+2007A>C
XM_011532867.2:c.2634+2007A>C XP_011531169.1:n.2634+2007A>C
XR_001738747.2:n.2696+2007A>C
XR_939685.2:n.2696+2007A>C
NM_000251.3:c.2734A>C MANE Select NP_000242.1:p.Lys912Gln