Canonical Allele Identifier: CA2499215999

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1049723
• ClinVar RCV Id: RCV001356195
• dbSNP Id: rs2103978746

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47408455del , CM000664.2:g.47408455del	GRCh38
NC_000002.11:g.47635594del , CM000664.1:g.47635594del	GRCh37
NC_000002.10:g.47489098del	NCBI36
NG_007110.2:g.10332del , LRG_218:g.10332del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.266del	ENSP00000495641.2:p.Val89GlufsTer?
ENST00000233146.7:c.266del MANE Select	ENSP00000233146.2:p.Val89GlufsTer?
ENST00000543555.6:c.68del	ENSP00000442697.1:p.Val23GlufsTer?
ENST00000644092.1:c.266del	ENSP00000496351.1:p.Val89GlufsTer?
ENST00000645339.1:c.266del	ENSP00000496441.1:p.Val89GlufsTer?
ENST00000645506.1:c.266del	ENSP00000495455.1:p.Val89GlufsTer?
ENST00000646415.1:c.266del	ENSP00000495543.1:p.Val89GlufsTer?
ENST00000233146.6:c.266del	ENSP00000233146.2:p.Val89GlufsTer?
ENST00000406134.5:c.266del	ENSP00000384199.1:p.Val89GlufsTer?
ENST00000454849.5:c.68del	ENSP00000411482.1:p.Val23GlufsTer?
ENST00000543555.5:c.68del	ENSP00000442697.1:p.Val23GlufsTer?
ENST00000610696.4:c.266del	ENSP00000483159.1:p.Val89GlufsTer?
ENST00000613514.4:c.266del	ENSP00000484137.1:p.Val89GlufsTer?
ENST00000617333.3:c.266del	ENSP00000482468.1:p.Val89GlufsTer?
ENST00000617938.4:c.266del	ENSP00000481158.1:p.Val89GlufsTer?
ENST00000621359.2:c.266del	ENSP00000481416.1:p.Val89GlufsTer?
NM_000251.2:c.266del , LRG_218t1:c.266del	NP_000242.1:p.Val89GlufsTer?
NM_001258281.1:c.68del	NP_001245210.1:p.Val23GlufsTer?
XM_005264332.2:c.266del	XP_005264389.2:p.Val89GlufsTer?
XM_011532867.1:c.266del	XP_011531169.1:p.Val89GlufsTer?
XR_939685.1:n.338del
XM_005264332.4:c.266del	XP_005264389.2:p.Val89GlufsTer?
XM_011532867.2:c.266del	XP_011531169.1:p.Val89GlufsTer?
XR_001738747.2:n.328del
XR_939685.2:n.328del
NM_000251.3:c.266del MANE Select	NP_000242.1:p.Val89GlufsTer?