Canonical Allele Identifier: CA3054211682

Gene: MSH2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482783del , CM000664.2:g.47482783del	GRCh38
NC_000002.11:g.47709922del , CM000664.1:g.47709922del	GRCh37
NC_000002.10:g.47563426del	NCBI36
NG_007110.2:g.84660del , LRG_218:g.84660del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+1912del	ENSP00000495641.2:n.2634+1912del
ENST00000233146.7:c.2639del MANE Select	ENSP00000233146.2:p.Gly880ValfsTer12
ENST00000543555.6:c.2441del	ENSP00000442697.1:p.Gly814ValfsTer12
ENST00000644092.1:c.*934+1912del	ENSP00000496351.1:n.*934+1912del
ENST00000644900.1:c.487+1912del
ENST00000645339.1:c.2634+1912del	ENSP00000496441.1:n.2634+1912del
ENST00000645506.1:c.2634+1912del	ENSP00000495455.1:n.2634+1912del
ENST00000646415.1:c.2634+1912del	ENSP00000495543.1:n.2634+1912del
ENST00000233146.6:c.2639del	ENSP00000233146.2:p.Gly880ValfsTer12
ENST00000406134.5:c.2634+1912del	ENSP00000384199.1:n.2634+1912del
ENST00000461394.5:n.75+1912del
ENST00000543555.5:c.2441del	ENSP00000442697.1:p.Gly814ValfsTer12
ENST00000610696.4:c.*1035del	ENSP00000483159.1:n.*1035del
ENST00000613514.4:c.*1179del	ENSP00000484137.1:n.*1179del
ENST00000617333.3:c.*1405del	ENSP00000482468.1:n.*1405del
ENST00000617938.4:c.*1611del	ENSP00000481158.1:n.*1611del
ENST00000621359.2:c.*205del	ENSP00000481416.1:n.*205del
NM_000251.2:c.2639del , LRG_218t1:c.2639del	NP_000242.1:p.Gly880ValfsTer12
NM_001258281.1:c.2441del	NP_001245210.1:p.Gly814ValfsTer12
XM_005264332.2:c.2634+1912del	XP_005264389.2:n.2634+1912del
XM_011532867.1:c.2634+1912del	XP_011531169.1:n.2634+1912del
XR_939685.1:n.2706+1912del
XM_005264332.4:c.2634+1912del	XP_005264389.2:n.2634+1912del
XM_011532867.2:c.2634+1912del	XP_011531169.1:n.2634+1912del
XR_001738747.2:n.2696+1912del
XR_939685.2:n.2696+1912del
NM_000251.3:c.2639del MANE Select	NP_000242.1:p.Gly880ValfsTer12