Canonical Allele Identifier: CA2699331896

Gene: MSH2

Linked Data

• dbSNP Id: rs2104436622

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480747dup , CM000664.2:g.47480747dup	GRCh38
NC_000002.11:g.47707886dup , CM000664.1:g.47707886dup	GRCh37
NC_000002.10:g.47561390dup	NCBI36
NG_007110.2:g.82624dup , LRG_218:g.82624dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2510dup	ENSP00000495641.2:p.Lys838Ter
ENST00000233146.7:c.2510dup MANE Select	ENSP00000233146.2:p.Lys838Ter
ENST00000543555.6:c.2312dup	ENSP00000442697.1:p.Lys772Ter
ENST00000644092.1:c.*810dup	ENSP00000496351.1:n.*810dup
ENST00000644900.1:c.363dup
ENST00000645339.1:c.2510dup	ENSP00000496441.1:p.Lys838Ter
ENST00000645506.1:c.2510dup	ENSP00000495455.1:p.Lys838Ter
ENST00000646415.1:c.2510dup	ENSP00000495543.1:p.Lys838Ter
ENST00000233146.6:c.2510dup	ENSP00000233146.2:p.Lys838Ter
ENST00000406134.5:c.2510dup	ENSP00000384199.1:p.Lys838Ter
ENST00000543555.5:c.2312dup	ENSP00000442697.1:p.Lys772Ter
ENST00000610696.4:c.*906dup	ENSP00000483159.1:n.*906dup
ENST00000613514.4:c.*1050dup	ENSP00000484137.1:n.*1050dup
ENST00000617333.3:c.*1276dup	ENSP00000482468.1:n.*1276dup
ENST00000617938.4:c.*1482dup	ENSP00000481158.1:n.*1482dup
ENST00000621359.2:c.*76dup	ENSP00000481416.1:n.*76dup
NM_000251.2:c.2510dup , LRG_218t1:c.2510dup	NP_000242.1:p.Lys838Ter
NM_001258281.1:c.2312dup	NP_001245210.1:p.Lys772Ter
XM_005264332.2:c.2510dup	XP_005264389.2:p.Lys838Ter
XM_011532867.1:c.2510dup	XP_011531169.1:p.Lys838Ter
XR_939685.1:n.2582dup
XM_005264332.4:c.2510dup	XP_005264389.2:p.Lys838Ter
XM_011532867.2:c.2510dup	XP_011531169.1:p.Lys838Ter
XR_001738747.2:n.2572dup
XR_939685.2:n.2572dup
NM_000251.3:c.2510dup MANE Select	NP_000242.1:p.Lys838Ter