Canonical Allele Identifier: CA019291

Gene: MSH2

Linked Data

• ClinVar Variation Id: 184645
• ClinVar RCV Id: RCV000163932 ; RCV000554840 ; RCV001267891
• dbSNP Id: rs786201590
• MyVariant Identifiers: chr2:g.47702188T>G (hg19) ; chr2:g.47475049T>G (hg38)
• PubMed: PMID:12454801 ; PMID:17531815 ; PMID:23990280

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475049T>G , CM000664.2:g.47475049T>G	GRCh38
NC_000002.11:g.47702188T>G , CM000664.1:g.47702188T>G	GRCh37
NC_000002.10:g.47555692T>G	NCBI36
NG_007110.2:g.76926T>G , LRG_218:g.76926T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1784T>G	ENSP00000495641.2:p.Leu595Arg
ENST00000233146.7:c.1784T>G MANE Select	ENSP00000233146.2:p.Leu595Arg
ENST00000543555.6:c.1586T>G	ENSP00000442697.1:p.Leu529Arg
ENST00000644092.1:c.*84T>G	ENSP00000496351.1:n.*84T>G
ENST00000645339.1:c.1784T>G	ENSP00000496441.1:p.Leu595Arg
ENST00000645506.1:c.1784T>G	ENSP00000495455.1:p.Leu595Arg
ENST00000646415.1:c.1784T>G	ENSP00000495543.1:p.Leu595Arg
ENST00000233146.6:c.1784T>G	ENSP00000233146.2:p.Leu595Arg
ENST00000406134.5:c.1784T>G	ENSP00000384199.1:p.Leu595Arg
ENST00000543555.5:c.1586T>G	ENSP00000442697.1:p.Leu529Arg
ENST00000610696.4:c.*180T>G	ENSP00000483159.1:n.*180T>G
ENST00000613514.4:c.*324T>G	ENSP00000484137.1:n.*324T>G
ENST00000617333.3:c.*550T>G	ENSP00000482468.1:n.*550T>G
ENST00000617938.4:c.*756T>G	ENSP00000481158.1:n.*756T>G
ENST00000621359.2:c.1784T>G	ENSP00000481416.1:p.Leu595Arg
NM_000251.2:c.1784T>G , LRG_218t1:c.1784T>G	NP_000242.1:p.Leu595Arg
NM_001258281.1:c.1586T>G	NP_001245210.1:p.Leu529Arg
XM_005264332.2:c.1784T>G	XP_005264389.2:p.Leu595Arg
XM_011532867.1:c.1784T>G	XP_011531169.1:p.Leu595Arg
XR_939685.1:n.1856T>G
XM_005264332.4:c.1784T>G	XP_005264389.2:p.Leu595Arg
XM_011532867.2:c.1784T>G	XP_011531169.1:p.Leu595Arg
XR_001738747.2:n.1846T>G
XR_939685.2:n.1846T>G
NM_000251.3:c.1784T>G MANE Select	NP_000242.1:p.Leu595Arg