Canonical Allele Identifier: CA16611057

Gene: MSH2

Linked Data

• ClinVar Variation Id: 408455
• ClinVar RCV Id: RCV000465186 ; RCV001201394 ; RCV002446811 ; RCV003449127
• dbSNP Id: rs1060501991
• MyVariant Identifiers: chr2:g.47707834G>A (hg19) ; chr2:g.47480695G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480695G>A , CM000664.2:g.47480695G>A	GRCh38
NC_000002.11:g.47707834G>A , CM000664.1:g.47707834G>A	GRCh37
NC_000002.10:g.47561338G>A	NCBI36
NG_007110.2:g.82572G>A , LRG_218:g.82572G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2459-1G>A	ENSP00000495641.2:n.2459-1G>A
ENST00000233146.7:c.2459-1G>A MANE Select	ENSP00000233146.2:n.2459-1G>A
ENST00000543555.6:c.2261-1G>A	ENSP00000442697.1:n.2261-1G>A
ENST00000644092.1:c.*759-1G>A	ENSP00000496351.1:n.*759-1G>A
ENST00000644900.1:c.312-1G>A
ENST00000645339.1:c.2459-1G>A	ENSP00000496441.1:n.2459-1G>A
ENST00000645506.1:c.2459-1G>A	ENSP00000495455.1:n.2459-1G>A
ENST00000646415.1:c.2459-1G>A	ENSP00000495543.1:n.2459-1G>A
ENST00000233146.6:c.2459-1G>A	ENSP00000233146.2:n.2459-1G>A
ENST00000406134.5:c.2459-1G>A	ENSP00000384199.1:n.2459-1G>A
ENST00000543555.5:c.2261-1G>A	ENSP00000442697.1:n.2261-1G>A
ENST00000610696.4:c.*855-1G>A	ENSP00000483159.1:n.*855-1G>A
ENST00000613514.4:c.*999-1G>A	ENSP00000484137.1:n.*999-1G>A
ENST00000617333.3:c.*1225-1G>A	ENSP00000482468.1:n.*1225-1G>A
ENST00000617938.4:c.*1431-1G>A	ENSP00000481158.1:n.*1431-1G>A
ENST00000621359.2:c.*25-1G>A	ENSP00000481416.1:n.*25-1G>A
NM_000251.2:c.2459-1G>A , LRG_218t1:c.2459-1G>A	NP_000242.1:n.2459-1G>A
NM_001258281.1:c.2261-1G>A	NP_001245210.1:n.2261-1G>A
XM_005264332.2:c.2459-1G>A	XP_005264389.2:n.2459-1G>A
XM_011532867.1:c.2459-1G>A	XP_011531169.1:n.2459-1G>A
XR_939685.1:n.2531-1G>A
XM_005264332.4:c.2459-1G>A	XP_005264389.2:n.2459-1G>A
XM_011532867.2:c.2459-1G>A	XP_011531169.1:n.2459-1G>A
XR_001738747.2:n.2521-1G>A
XR_939685.2:n.2521-1G>A
NM_000251.3:c.2459-1G>A MANE Select	NP_000242.1:n.2459-1G>A