Canonical Allele Identifier: CA10588344

Gene: MSH2

Linked Data

• ClinVar Variation Id: 265573
• ClinVar RCV Id: RCV000256112 ; RCV000491622 ; RCV000506471 ; RCV000629692 ; RCV003454782
• dbSNP Id: rs28929483
• MyVariant Identifiers: chr2:g.47702269C>G (hg19) ; chr2:g.47475130C>G (hg38)
• PubMed: PMID:8062247 ; PMID:22102614 ; PMID:24362816 ; PMID:26951660 ; PMID:28874130

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475130C>G , CM000664.2:g.47475130C>G	GRCh38
NC_000002.11:g.47702269C>G , CM000664.1:g.47702269C>G	GRCh37
NC_000002.10:g.47555773C>G	NCBI36
NG_007110.2:g.77007C>G , LRG_218:g.77007C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1865C>G	ENSP00000495641.2:p.Pro622Arg
ENST00000233146.7:c.1865C>G MANE Select	ENSP00000233146.2:p.Pro622Arg
ENST00000543555.6:c.1667C>G	ENSP00000442697.1:p.Pro556Arg
ENST00000644092.1:c.*165C>G	ENSP00000496351.1:n.*165C>G
ENST00000645339.1:c.1865C>G	ENSP00000496441.1:p.Pro622Arg
ENST00000645506.1:c.1865C>G	ENSP00000495455.1:p.Pro622Arg
ENST00000646415.1:c.1865C>G	ENSP00000495543.1:p.Pro622Arg
ENST00000233146.6:c.1865C>G	ENSP00000233146.2:p.Pro622Arg
ENST00000406134.5:c.1865C>G	ENSP00000384199.1:p.Pro622Arg
ENST00000543555.5:c.1667C>G	ENSP00000442697.1:p.Pro556Arg
ENST00000610696.4:c.*261C>G	ENSP00000483159.1:n.*261C>G
ENST00000613514.4:c.*405C>G	ENSP00000484137.1:n.*405C>G
ENST00000617333.3:c.*631C>G	ENSP00000482468.1:n.*631C>G
ENST00000617938.4:c.*837C>G	ENSP00000481158.1:n.*837C>G
ENST00000621359.2:c.1865C>G	ENSP00000481416.1:p.Pro622Arg
NM_000251.2:c.1865C>G , LRG_218t1:c.1865C>G	NP_000242.1:p.Pro622Arg
NM_001258281.1:c.1667C>G	NP_001245210.1:p.Pro556Arg
XM_005264332.2:c.1865C>G	XP_005264389.2:p.Pro622Arg
XM_011532867.1:c.1865C>G	XP_011531169.1:p.Pro622Arg
XR_939685.1:n.1937C>G
XM_005264332.4:c.1865C>G	XP_005264389.2:p.Pro622Arg
XM_011532867.2:c.1865C>G	XP_011531169.1:p.Pro622Arg
XR_001738747.2:n.1927C>G
XR_939685.2:n.1927C>G
NM_000251.3:c.1865C>G MANE Select	NP_000242.1:p.Pro622Arg