Canonical Allele Identifier: CA2495872355

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475007_47475013delinsGTTTTTA , CM000664.2:g.47475007_47475013delinsGTTTTTA	GRCh38
NC_000002.11:g.47702146_47702152delinsGTTTTTA , CM000664.1:g.47702146_47702152delinsGTTTTTA	GRCh37
NC_000002.10:g.47555650_47555656delinsGTTTTTA	NCBI36
NG_007110.2:g.76884_76890delinsGTTTTTA , LRG_218:g.76884_76890delinsGTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1760-18_1760-12delinsGTTTTTA	ENSP00000495641.2:n.1760-18_1760-12delinsGTTTTTA
ENST00000233146.7:c.1760-18_1760-12delinsGTTTTTA MANE Select	ENSP00000233146.2:n.1760-18_1760-12delinsGTTTTTA
ENST00000543555.6:c.1562-18_1562-12delinsGTTTTTA	ENSP00000442697.1:n.1562-18_1562-12delinsGTTTTTA
ENST00000644092.1:c.*60-18_*60-12delinsGTTTTTA	ENSP00000496351.1:n.*60-18_*60-12delinsGTTTTTA
ENST00000645339.1:c.1760-18_1760-12delinsGTTTTTA	ENSP00000496441.1:n.1760-18_1760-12delinsGTTTTTA
ENST00000645506.1:c.1760-18_1760-12delinsGTTTTTA	ENSP00000495455.1:n.1760-18_1760-12delinsGTTTTTA
ENST00000646415.1:c.1760-18_1760-12delinsGTTTTTA	ENSP00000495543.1:n.1760-18_1760-12delinsGTTTTTA
ENST00000233146.6:c.1760-18_1760-12delinsGTTTTTA	ENSP00000233146.2:n.1760-18_1760-12delinsGTTTTTA
ENST00000406134.5:c.1760-18_1760-12delinsGTTTTTA	ENSP00000384199.1:n.1760-18_1760-12delinsGTTTTTA
ENST00000543555.5:c.1562-18_1562-12delinsGTTTTTA	ENSP00000442697.1:n.1562-18_1562-12delinsGTTTTTA
ENST00000610696.4:c.*156-18_*156-12delinsGTTTTTA	ENSP00000483159.1:n.*156-18_*156-12delinsGTTTTTA
ENST00000613514.4:c.*300-18_*300-12delinsGTTTTTA	ENSP00000484137.1:n.*300-18_*300-12delinsGTTTTTA
ENST00000617333.3:c.*526-18_*526-12delinsGTTTTTA	ENSP00000482468.1:n.*526-18_*526-12delinsGTTTTTA
ENST00000617938.4:c.*732-18_*732-12delinsGTTTTTA	ENSP00000481158.1:n.*732-18_*732-12delinsGTTTTTA
ENST00000621359.2:c.1760-18_1760-12delinsGTTTTTA	ENSP00000481416.1:n.1760-18_1760-12delinsGTTTTTA
NM_000251.2:c.1760-18_1760-12delinsGTTTTTA , LRG_218t1:c.1760-18_1760-12delinsGTTTTTA	NP_000242.1:n.1760-18_1760-12delinsGTTTTTA
NM_001258281.1:c.1562-18_1562-12delinsGTTTTTA	NP_001245210.1:n.1562-18_1562-12delinsGTTTTTA
XM_005264332.2:c.1760-18_1760-12delinsGTTTTTA	XP_005264389.2:n.1760-18_1760-12delinsGTTTTTA
XM_011532867.1:c.1760-18_1760-12delinsGTTTTTA	XP_011531169.1:n.1760-18_1760-12delinsGTTTTTA
XR_939685.1:n.1832-18_1832-12delinsGTTTTTA
XM_005264332.4:c.1760-18_1760-12delinsGTTTTTA	XP_005264389.2:n.1760-18_1760-12delinsGTTTTTA
XM_011532867.2:c.1760-18_1760-12delinsGTTTTTA	XP_011531169.1:n.1760-18_1760-12delinsGTTTTTA
XR_001738747.2:n.1822-18_1822-12delinsGTTTTTA
XR_939685.2:n.1822-18_1822-12delinsGTTTTTA
NM_000251.3:c.1760-18_1760-12delinsGTTTTTA MANE Select	NP_000242.1:n.1760-18_1760-12delinsGTTTTTA