Canonical Allele Identifier: CA346732951

Gene: MSH2

Linked Data

• ClinVar Variation Id: 455622
• ClinVar RCV Id: RCV000527981 ; RCV000573534 ; RCV001800735 ; RCV003470714 ; RCV004003755
• dbSNP Id: rs876660115
• gnomAD v4: 2-47414380-T-A
• MyVariant Identifiers: chr2:g.47641519T>A (hg19) ; chr2:g.47414380T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414380T>A , CM000664.2:g.47414380T>A	GRCh38
NC_000002.11:g.47641519T>A , CM000664.1:g.47641519T>A	GRCh37
NC_000002.10:g.47495023T>A	NCBI36
NG_007110.2:g.16257T>A , LRG_218:g.16257T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.904T>A	ENSP00000495641.2:p.Leu302Met
ENST00000233146.7:c.904T>A MANE Select	ENSP00000233146.2:p.Leu302Met
ENST00000543555.6:c.706T>A	ENSP00000442697.1:p.Leu236Met
ENST00000644092.1:c.904T>A	ENSP00000496351.1:p.Leu302Met
ENST00000645339.1:c.904T>A	ENSP00000496441.1:p.Leu302Met
ENST00000645506.1:c.904T>A	ENSP00000495455.1:p.Leu302Met
ENST00000646415.1:c.904T>A	ENSP00000495543.1:p.Leu302Met
ENST00000233146.6:c.904T>A	ENSP00000233146.2:p.Leu302Met
ENST00000406134.5:c.904T>A	ENSP00000384199.1:p.Leu302Met
ENST00000543555.5:c.706T>A	ENSP00000442697.1:p.Leu236Met
ENST00000610696.4:c.904T>A	ENSP00000483159.1:p.Leu302Met
ENST00000613514.4:c.904T>A	ENSP00000484137.1:p.Leu302Met
ENST00000617333.3:c.904T>A	ENSP00000482468.1:p.Leu302Met
ENST00000617938.4:c.904T>A	ENSP00000481158.1:p.Leu302Met
ENST00000621359.2:c.904T>A	ENSP00000481416.1:p.Leu302Met
NM_000251.2:c.904T>A , LRG_218t1:c.904T>A	NP_000242.1:p.Leu302Met
NM_001258281.1:c.706T>A	NP_001245210.1:p.Leu236Met
XM_005264332.2:c.904T>A	XP_005264389.2:p.Leu302Met
XM_011532867.1:c.904T>A	XP_011531169.1:p.Leu302Met
XR_939685.1:n.976T>A
XM_005264332.4:c.904T>A	XP_005264389.2:p.Leu302Met
XM_011532867.2:c.904T>A	XP_011531169.1:p.Leu302Met
XR_001738747.2:n.966T>A
XR_939685.2:n.966T>A
NM_000251.3:c.904T>A MANE Select	NP_000242.1:p.Leu302Met