Canonical Allele Identifier: CA346729973

Gene: MSH2

Linked Data

• ClinVar Variation Id: 2453482
• ClinVar RCV Id: RCV003182937
• dbSNP Id: rs1553369759
• MyVariant Identifiers: chr2:g.47705553C>G (hg19) ; chr2:g.47478414C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478414C>G , CM000664.2:g.47478414C>G	GRCh38
NC_000002.11:g.47705553C>G , CM000664.1:g.47705553C>G	GRCh37
NC_000002.10:g.47559057C>G	NCBI36
NG_007110.2:g.80291C>G , LRG_218:g.80291C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2353C>G	ENSP00000495641.2:p.His785Asp
ENST00000233146.7:c.2353C>G MANE Select	ENSP00000233146.2:p.His785Asp
ENST00000543555.6:c.2155C>G	ENSP00000442697.1:p.His719Asp
ENST00000644092.1:c.*653C>G	ENSP00000496351.1:n.*653C>G
ENST00000644900.1:c.206C>G
ENST00000645339.1:c.2353C>G	ENSP00000496441.1:p.His785Asp
ENST00000645506.1:c.2353C>G	ENSP00000495455.1:p.His785Asp
ENST00000646415.1:c.2353C>G	ENSP00000495543.1:p.His785Asp
ENST00000233146.6:c.2353C>G	ENSP00000233146.2:p.His785Asp
ENST00000406134.5:c.2353C>G	ENSP00000384199.1:p.His785Asp
ENST00000543555.5:c.2155C>G	ENSP00000442697.1:p.His719Asp
ENST00000610696.4:c.*749C>G	ENSP00000483159.1:n.*749C>G
ENST00000613514.4:c.*893C>G	ENSP00000484137.1:n.*893C>G
ENST00000617333.3:c.*1119C>G	ENSP00000482468.1:n.*1119C>G
ENST00000617938.4:c.*1325C>G	ENSP00000481158.1:n.*1325C>G
ENST00000621359.2:c.2352C>G	ENSP00000481416.1:p.Phe784Leu
NM_000251.2:c.2353C>G , LRG_218t1:c.2353C>G	NP_000242.1:p.His785Asp
NM_001258281.1:c.2155C>G	NP_001245210.1:p.His719Asp
XM_005264332.2:c.2353C>G	XP_005264389.2:p.His785Asp
XM_011532867.1:c.2353C>G	XP_011531169.1:p.His785Asp
XR_939685.1:n.2425C>G
XM_005264332.4:c.2353C>G	XP_005264389.2:p.His785Asp
XM_011532867.2:c.2353C>G	XP_011531169.1:p.His785Asp
XR_001738747.2:n.2415C>G
XR_939685.2:n.2415C>G
NM_000251.3:c.2353C>G MANE Select	NP_000242.1:p.His785Asp