Canonical Allele Identifier: CA2573134865

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1458081
• ClinVar RCV Id: RCV001972793
• dbSNP Id: rs2104343300

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475146dup , CM000664.2:g.47475146dup	GRCh38
NC_000002.11:g.47702285dup , CM000664.1:g.47702285dup	GRCh37
NC_000002.10:g.47555789dup	NCBI36
NG_007110.2:g.77023dup , LRG_218:g.77023dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1881dup	ENSP00000495641.2:p.Gly628ArgfsTer16
ENST00000233146.7:c.1881dup MANE Select	ENSP00000233146.2:p.Gly628ArgfsTer16
ENST00000543555.6:c.1683dup	ENSP00000442697.1:p.Gly562ArgfsTer16
ENST00000644092.1:c.*181dup	ENSP00000496351.1:n.*181dup
ENST00000645339.1:c.1881dup	ENSP00000496441.1:p.Gly628ArgfsTer16
ENST00000645506.1:c.1881dup	ENSP00000495455.1:p.Gly628ArgfsTer16
ENST00000646415.1:c.1881dup	ENSP00000495543.1:p.Gly628ArgfsTer16
ENST00000233146.6:c.1881dup	ENSP00000233146.2:p.Gly628ArgfsTer16
ENST00000406134.5:c.1881dup	ENSP00000384199.1:p.Gly628ArgfsTer16
ENST00000543555.5:c.1683dup	ENSP00000442697.1:p.Gly562ArgfsTer16
ENST00000610696.4:c.*277dup	ENSP00000483159.1:n.*277dup
ENST00000613514.4:c.*421dup	ENSP00000484137.1:n.*421dup
ENST00000617333.3:c.*647dup	ENSP00000482468.1:n.*647dup
ENST00000617938.4:c.*853dup	ENSP00000481158.1:n.*853dup
ENST00000621359.2:c.1881dup	ENSP00000481416.1:p.Gly628ArgfsTer16
NM_000251.2:c.1881dup , LRG_218t1:c.1881dup	NP_000242.1:p.Gly628ArgfsTer16
NM_001258281.1:c.1683dup	NP_001245210.1:p.Gly562ArgfsTer16
XM_005264332.2:c.1881dup	XP_005264389.2:p.Gly628ArgfsTer16
XM_011532867.1:c.1881dup	XP_011531169.1:p.Gly628ArgfsTer16
XR_939685.1:n.1953dup
XM_005264332.4:c.1881dup	XP_005264389.2:p.Gly628ArgfsTer16
XM_011532867.2:c.1881dup	XP_011531169.1:p.Gly628ArgfsTer16
XR_001738747.2:n.1943dup
XR_939685.2:n.1943dup
NM_000251.3:c.1881dup MANE Select	NP_000242.1:p.Gly628ArgfsTer16