Canonical Allele Identifier: CA019418

Gene: MSH2

Linked Data

• ClinVar Variation Id: 90799
• ClinVar RCV Id: RCV000076300 ; RCV000202183 ; RCV000491040 ; RCV000629963 ; RCV001357329 ; RCV003452860
• dbSNP Id: rs63750493
• MyVariant Identifiers: chr2:g.47702239C>G (hg19) ; chr2:g.47475100C>G (hg38)
• PubMed: PMID:15849733 ; PMID:16636019

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475100C>G , CM000664.2:g.47475100C>G	GRCh38
NC_000002.11:g.47702239C>G , CM000664.1:g.47702239C>G	GRCh37
NC_000002.10:g.47555743C>G	NCBI36
NG_007110.2:g.76977C>G , LRG_218:g.76977C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1835C>G	ENSP00000495641.2:p.Ser612Ter
ENST00000233146.7:c.1835C>G MANE Select	ENSP00000233146.2:p.Ser612Ter
ENST00000543555.6:c.1637C>G	ENSP00000442697.1:p.Ser546Ter
ENST00000644092.1:c.*135C>G	ENSP00000496351.1:n.*135C>G
ENST00000645339.1:c.1835C>G	ENSP00000496441.1:p.Ser612Ter
ENST00000645506.1:c.1835C>G	ENSP00000495455.1:p.Ser612Ter
ENST00000646415.1:c.1835C>G	ENSP00000495543.1:p.Ser612Ter
ENST00000233146.6:c.1835C>G	ENSP00000233146.2:p.Ser612Ter
ENST00000406134.5:c.1835C>G	ENSP00000384199.1:p.Ser612Ter
ENST00000543555.5:c.1637C>G	ENSP00000442697.1:p.Ser546Ter
ENST00000610696.4:c.*231C>G	ENSP00000483159.1:n.*231C>G
ENST00000613514.4:c.*375C>G	ENSP00000484137.1:n.*375C>G
ENST00000617333.3:c.*601C>G	ENSP00000482468.1:n.*601C>G
ENST00000617938.4:c.*807C>G	ENSP00000481158.1:n.*807C>G
ENST00000621359.2:c.1835C>G	ENSP00000481416.1:p.Ser612Ter
NM_000251.2:c.1835C>G , LRG_218t1:c.1835C>G	NP_000242.1:p.Ser612Ter
NM_001258281.1:c.1637C>G	NP_001245210.1:p.Ser546Ter
XM_005264332.2:c.1835C>G	XP_005264389.2:p.Ser612Ter
XM_011532867.1:c.1835C>G	XP_011531169.1:p.Ser612Ter
XR_939685.1:n.1907C>G
XM_005264332.4:c.1835C>G	XP_005264389.2:p.Ser612Ter
XM_011532867.2:c.1835C>G	XP_011531169.1:p.Ser612Ter
XR_001738747.2:n.1897C>G
XR_939685.2:n.1897C>G
NM_000251.3:c.1835C>G MANE Select	NP_000242.1:p.Ser612Ter