Canonical Allele Identifier: CA016843

Gene: MSH2

Linked Data

• ClinVar Variation Id: 90503
• ClinVar RCV Id: RCV000500876 ; RCV002345383 ; RCV002228181 ; RCV003452795
• dbSNP Id: rs63751004
• MyVariant Identifiers: chr2:g.47643504G>A (hg19) ; chr2:g.47416365G>A (hg38)
• ERepo: CA016843/MONDO:0005835/137
• PubMed: PMID:16995940 ; PMID:17720936 ; PMID:18383312

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47416365G>A , CM000664.2:g.47416365G>A	GRCh38
NC_000002.11:g.47643504G>A , CM000664.1:g.47643504G>A	GRCh37
NC_000002.10:g.47497008G>A	NCBI36
NG_007110.2:g.18242G>A , LRG_218:g.18242G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1012G>A	ENSP00000495641.2:p.Gly338Arg
ENST00000233146.7:c.1012G>A MANE Select	ENSP00000233146.2:p.Gly338Arg
ENST00000543555.6:c.814G>A	ENSP00000442697.1:p.Gly272Arg
ENST00000644092.1:c.1012G>A	ENSP00000496351.1:p.Gly338Arg
ENST00000645339.1:c.1012G>A	ENSP00000496441.1:p.Gly338Arg
ENST00000645506.1:c.1012G>A	ENSP00000495455.1:p.Gly338Arg
ENST00000646415.1:c.1012G>A	ENSP00000495543.1:p.Gly338Arg
ENST00000233146.6:c.1012G>A	ENSP00000233146.2:p.Gly338Arg
ENST00000406134.5:c.1012G>A	ENSP00000384199.1:p.Gly338Arg
ENST00000543555.5:c.814G>A	ENSP00000442697.1:p.Gly272Arg
ENST00000610696.4:c.1012G>A	ENSP00000483159.1:p.Gly338Arg
ENST00000613514.4:c.1012G>A	ENSP00000484137.1:p.Gly338Arg
ENST00000617333.3:c.1012G>A	ENSP00000482468.1:p.Gly338Arg
ENST00000617938.4:c.1012G>A	ENSP00000481158.1:p.Gly338Arg
ENST00000621359.2:c.1012G>A	ENSP00000481416.1:p.Gly338Arg
NM_000251.2:c.1012G>A , LRG_218t1:c.1012G>A	NP_000242.1:p.Gly338Arg
NM_001258281.1:c.814G>A	NP_001245210.1:p.Gly272Arg
XM_005264332.2:c.1012G>A	XP_005264389.2:p.Gly338Arg
XM_011532867.1:c.1012G>A	XP_011531169.1:p.Gly338Arg
XR_939685.1:n.1084G>A
XM_005264332.4:c.1012G>A	XP_005264389.2:p.Gly338Arg
XM_011532867.2:c.1012G>A	XP_011531169.1:p.Gly338Arg
XR_001738747.2:n.1074G>A
XR_939685.2:n.1074G>A
NM_000251.3:c.1012G>A MANE Select	NP_000242.1:p.Gly338Arg