Canonical Allele Identifier: CA020844

Gene: MSH2

Linked Data

• ClinVar Variation Id: 91021
• ClinVar RCV Id: RCV000076523 ; RCV000491856 ; RCV000519129 ; RCV000791439 ; RCV001255522 ; RCV003452927
• dbSNP Id: rs63751624
• MyVariant Identifiers: chr2:g.47708010G>A (hg19) ; chr2:g.47480871G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480871G>A , CM000664.2:g.47480871G>A	GRCh38
NC_000002.11:g.47708010G>A , CM000664.1:g.47708010G>A	GRCh37
NC_000002.10:g.47561514G>A	NCBI36
NG_007110.2:g.82748G>A , LRG_218:g.82748G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634G>A	ENSP00000495641.2:p.Glu878=
ENST00000233146.7:c.2634G>A MANE Select	ENSP00000233146.2:p.Glu878=
ENST00000543555.6:c.2436G>A	ENSP00000442697.1:p.Glu812=
ENST00000644092.1:c.*934G>A	ENSP00000496351.1:n.*934G>A
ENST00000644900.1:c.487G>A
ENST00000645339.1:c.2634G>A	ENSP00000496441.1:p.Glu878=
ENST00000645506.1:c.2634G>A	ENSP00000495455.1:p.Glu878=
ENST00000646415.1:c.2634G>A	ENSP00000495543.1:p.Glu878=
ENST00000233146.6:c.2634G>A	ENSP00000233146.2:p.Glu878=
ENST00000406134.5:c.2634G>A	ENSP00000384199.1:p.Glu878=
ENST00000461394.5:n.75G>A
ENST00000543555.5:c.2436G>A	ENSP00000442697.1:p.Glu812=
ENST00000610696.4:c.*1030G>A	ENSP00000483159.1:n.*1030G>A
ENST00000613514.4:c.*1174G>A	ENSP00000484137.1:n.*1174G>A
ENST00000617333.3:c.*1400G>A	ENSP00000482468.1:n.*1400G>A
ENST00000617938.4:c.*1606G>A	ENSP00000481158.1:n.*1606G>A
ENST00000621359.2:c.*200G>A	ENSP00000481416.1:n.*200G>A
NM_000251.2:c.2634G>A , LRG_218t1:c.2634G>A	NP_000242.1:p.Glu878=
NM_001258281.1:c.2436G>A	NP_001245210.1:p.Glu812=
XM_005264332.2:c.2634G>A	XP_005264389.2:p.Glu878=
XM_011532867.1:c.2634G>A	XP_011531169.1:p.Glu878=
XR_939685.1:n.2706G>A
XM_005264332.4:c.2634G>A	XP_005264389.2:p.Glu878=
XM_011532867.2:c.2634G>A	XP_011531169.1:p.Glu878=
XR_001738747.2:n.2696G>A
XR_939685.2:n.2696G>A
NM_000251.3:c.2634G>A MANE Select	NP_000242.1:p.Glu878=