Canonical Allele Identifier: CA346729166
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1324737
ClinVar RCV Id: RCV001782457
dbSNP Id: rs1573569964

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47476423A>G , CM000664.2:g.47476423A>G GRCh38
NC_000002.11:g.47703562A>G , CM000664.1:g.47703562A>G GRCh37
NC_000002.10:g.47557066A>G NCBI36
NG_007110.2:g.78300A>G , LRG_218:g.78300A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.2062A>G ENSP00000495641.2:p.Met688Val
ENST00000233146.7:c.2062A>G MANE Select ENSP00000233146.2:p.Met688Val
ENST00000543555.6:c.1864A>G ENSP00000442697.1:p.Met622Val
ENST00000644092.1:c.*362A>G ENSP00000496351.1:n.*362A>G
ENST00000645339.1:c.2062A>G ENSP00000496441.1:p.Met688Val
ENST00000645506.1:c.2062A>G ENSP00000495455.1:p.Met688Val
ENST00000646415.1:c.2062A>G ENSP00000495543.1:p.Met688Val
ENST00000233146.6:c.2062A>G ENSP00000233146.2:p.Met688Val
ENST00000406134.5:c.2062A>G ENSP00000384199.1:p.Met688Val
ENST00000543555.5:c.1864A>G ENSP00000442697.1:p.Met622Val
ENST00000610696.4:c.*458A>G ENSP00000483159.1:n.*458A>G
ENST00000613514.4:c.*602A>G ENSP00000484137.1:n.*602A>G
ENST00000617333.3:c.*828A>G ENSP00000482468.1:n.*828A>G
ENST00000617938.4:c.*1034A>G ENSP00000481158.1:n.*1034A>G
ENST00000621359.2:c.2062A>G ENSP00000481416.1:p.Met688Val
NM_000251.2:c.2062A>G , LRG_218t1:c.2062A>G NP_000242.1:p.Met688Val
NM_001258281.1:c.1864A>G NP_001245210.1:p.Met622Val
XM_005264332.2:c.2062A>G XP_005264389.2:p.Met688Val
XM_011532867.1:c.2062A>G XP_011531169.1:p.Met688Val
XR_939685.1:n.2134A>G
XM_005264332.4:c.2062A>G XP_005264389.2:p.Met688Val
XM_011532867.2:c.2062A>G XP_011531169.1:p.Met688Val
XR_001738747.2:n.2124A>G
XR_939685.2:n.2124A>G
NM_000251.3:c.2062A>G MANE Select NP_000242.1:p.Met688Val