Canonical Allele Identifier: CA2495872329

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47474972_47474974delinsCTG , CM000664.2:g.47474972_47474974delinsCTG	GRCh38
NC_000002.11:g.47702111_47702113delinsCTG , CM000664.1:g.47702111_47702113delinsCTG	GRCh37
NC_000002.10:g.47555615_47555617delinsCTG	NCBI36
NG_007110.2:g.76849_76851delinsCTG , LRG_218:g.76849_76851delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1760-53_1760-51delinsCTG	ENSP00000495641.2:n.1760-53_1760-51delinsCTG
ENST00000233146.7:c.1760-53_1760-51delinsCTG MANE Select	ENSP00000233146.2:n.1760-53_1760-51delinsCTG
ENST00000543555.6:c.1562-53_1562-51delinsCTG	ENSP00000442697.1:n.1562-53_1562-51delinsCTG
ENST00000644092.1:c.*60-53_*60-51delinsCTG	ENSP00000496351.1:n.*60-53_*60-51delinsCTG
ENST00000645339.1:c.1760-53_1760-51delinsCTG	ENSP00000496441.1:n.1760-53_1760-51delinsCTG
ENST00000645506.1:c.1760-53_1760-51delinsCTG	ENSP00000495455.1:n.1760-53_1760-51delinsCTG
ENST00000646415.1:c.1760-53_1760-51delinsCTG	ENSP00000495543.1:n.1760-53_1760-51delinsCTG
ENST00000233146.6:c.1760-53_1760-51delinsCTG	ENSP00000233146.2:n.1760-53_1760-51delinsCTG
ENST00000406134.5:c.1760-53_1760-51delinsCTG	ENSP00000384199.1:n.1760-53_1760-51delinsCTG
ENST00000543555.5:c.1562-53_1562-51delinsCTG	ENSP00000442697.1:n.1562-53_1562-51delinsCTG
ENST00000610696.4:c.*156-53_*156-51delinsCTG	ENSP00000483159.1:n.*156-53_*156-51delinsCTG
ENST00000613514.4:c.*300-53_*300-51delinsCTG	ENSP00000484137.1:n.*300-53_*300-51delinsCTG
ENST00000617333.3:c.*526-53_*526-51delinsCTG	ENSP00000482468.1:n.*526-53_*526-51delinsCTG
ENST00000617938.4:c.*732-53_*732-51delinsCTG	ENSP00000481158.1:n.*732-53_*732-51delinsCTG
ENST00000621359.2:c.1760-53_1760-51delinsCTG	ENSP00000481416.1:n.1760-53_1760-51delinsCTG
NM_000251.2:c.1760-53_1760-51delinsCTG , LRG_218t1:c.1760-53_1760-51delinsCTG	NP_000242.1:n.1760-53_1760-51delinsCTG
NM_001258281.1:c.1562-53_1562-51delinsCTG	NP_001245210.1:n.1562-53_1562-51delinsCTG
XM_005264332.2:c.1760-53_1760-51delinsCTG	XP_005264389.2:n.1760-53_1760-51delinsCTG
XM_011532867.1:c.1760-53_1760-51delinsCTG	XP_011531169.1:n.1760-53_1760-51delinsCTG
XR_939685.1:n.1832-53_1832-51delinsCTG
XM_005264332.4:c.1760-53_1760-51delinsCTG	XP_005264389.2:n.1760-53_1760-51delinsCTG
XM_011532867.2:c.1760-53_1760-51delinsCTG	XP_011531169.1:n.1760-53_1760-51delinsCTG
XR_001738747.2:n.1822-53_1822-51delinsCTG
XR_939685.2:n.1822-53_1822-51delinsCTG
NM_000251.3:c.1760-53_1760-51delinsCTG MANE Select	NP_000242.1:n.1760-53_1760-51delinsCTG