Canonical Allele Identifier: CA645369222

Gene: MSH2

Linked Data

• ClinVar Variation Id: 428476
• ClinVar RCV Id: RCV000491415
• dbSNP Id: rs1114167823
• MyVariant Identifiers: chr2:g.47702334del (hg19) ; chr2:g.47475195del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475195del , CM000664.2:g.47475195del	GRCh38
NC_000002.11:g.47702334del , CM000664.1:g.47702334del	GRCh37
NC_000002.10:g.47555838del	NCBI36
NG_007110.2:g.77072del , LRG_218:g.77072del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1930del	ENSP00000495641.2:p.Val644PhefsTer?
ENST00000233146.7:c.1930del MANE Select	ENSP00000233146.2:p.Val644PhefsTer?
ENST00000543555.6:c.1732del	ENSP00000442697.1:p.Val578PhefsTer?
ENST00000644092.1:c.*230del	ENSP00000496351.1:n.*230del
ENST00000645339.1:c.1930del	ENSP00000496441.1:p.Val644PhefsTer?
ENST00000645506.1:c.1930del	ENSP00000495455.1:p.Val644PhefsTer?
ENST00000646415.1:c.1930del	ENSP00000495543.1:p.Val644PhefsTer?
ENST00000233146.6:c.1930del	ENSP00000233146.2:p.Val644PhefsTer?
ENST00000406134.5:c.1930del	ENSP00000384199.1:p.Val644PhefsTer?
ENST00000543555.5:c.1732del	ENSP00000442697.1:p.Val578PhefsTer?
ENST00000610696.4:c.*326del	ENSP00000483159.1:n.*326del
ENST00000613514.4:c.*470del	ENSP00000484137.1:n.*470del
ENST00000617333.3:c.*696del	ENSP00000482468.1:n.*696del
ENST00000617938.4:c.*902del	ENSP00000481158.1:n.*902del
ENST00000621359.2:c.1930del	ENSP00000481416.1:p.Val644PhefsTer?
NM_000251.2:c.1930del , LRG_218t1:c.1930del	NP_000242.1:p.Val644PhefsTer?
NM_001258281.1:c.1732del	NP_001245210.1:p.Val578PhefsTer?
XM_005264332.2:c.1930del	XP_005264389.2:p.Val644PhefsTer?
XM_011532867.1:c.1930del	XP_011531169.1:p.Val644PhefsTer?
XR_939685.1:n.2002del
XM_005264332.4:c.1930del	XP_005264389.2:p.Val644PhefsTer?
XM_011532867.2:c.1930del	XP_011531169.1:p.Val644PhefsTer?
XR_001738747.2:n.1992del
XR_939685.2:n.1992del
NM_000251.3:c.1930del MANE Select	NP_000242.1:p.Val644PhefsTer?