Canonical Allele Identifier: CA346731413

Gene: MSH2

Linked Data

• dbSNP Id: rs1230083633
• gnomAD v2: 2-47709939-G-C
• gnomAD v4: 2-47482800-G-C
• MyVariant Identifiers: chr2:g.47709939G>C (hg19) ; chr2:g.47482800G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482800G>C , CM000664.2:g.47482800G>C	GRCh38
NC_000002.11:g.47709939G>C , CM000664.1:g.47709939G>C	GRCh37
NC_000002.10:g.47563443G>C	NCBI36
NG_007110.2:g.84677G>C , LRG_218:g.84677G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.2634+1929G>C	ENSP00000495641.2:n.2634+1929G>C
ENST00000233146.7:c.2656G>C MANE Select	ENSP00000233146.2:p.Glu886Gln
ENST00000543555.6:c.2458G>C	ENSP00000442697.1:p.Glu820Gln
ENST00000644092.1:c.*934+1929G>C	ENSP00000496351.1:n.*934+1929G>C
ENST00000644900.1:c.487+1929G>C
ENST00000645339.1:c.2634+1929G>C	ENSP00000496441.1:n.2634+1929G>C
ENST00000645506.1:c.2634+1929G>C	ENSP00000495455.1:n.2634+1929G>C
ENST00000646415.1:c.2634+1929G>C	ENSP00000495543.1:n.2634+1929G>C
ENST00000233146.6:c.2656G>C	ENSP00000233146.2:p.Glu886Gln
ENST00000406134.5:c.2634+1929G>C	ENSP00000384199.1:n.2634+1929G>C
ENST00000461394.5:n.75+1929G>C
ENST00000543555.5:c.2458G>C	ENSP00000442697.1:p.Glu820Gln
ENST00000610696.4:c.*1052G>C	ENSP00000483159.1:n.*1052G>C
ENST00000613514.4:c.*1196G>C	ENSP00000484137.1:n.*1196G>C
ENST00000617333.3:c.*1422G>C	ENSP00000482468.1:n.*1422G>C
ENST00000617938.4:c.*1628G>C	ENSP00000481158.1:n.*1628G>C
ENST00000621359.2:c.*222G>C	ENSP00000481416.1:n.*222G>C
NM_000251.2:c.2656G>C , LRG_218t1:c.2656G>C	NP_000242.1:p.Glu886Gln
NM_001258281.1:c.2458G>C	NP_001245210.1:p.Glu820Gln
XM_005264332.2:c.2634+1929G>C	XP_005264389.2:n.2634+1929G>C
XM_011532867.1:c.2634+1929G>C	XP_011531169.1:n.2634+1929G>C
XR_939685.1:n.2706+1929G>C
XM_005264332.4:c.2634+1929G>C	XP_005264389.2:n.2634+1929G>C
XM_011532867.2:c.2634+1929G>C	XP_011531169.1:n.2634+1929G>C
XR_001738747.2:n.2696+1929G>C
XR_939685.2:n.2696+1929G>C
NM_000251.3:c.2656G>C MANE Select	NP_000242.1:p.Glu886Gln