Canonical Allele Identifier: CA2576961005

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480608del , CM000664.2:g.47480608del	GRCh38
NC_000002.11:g.47707747del , CM000664.1:g.47707747del	GRCh37
NC_000002.10:g.47561251del	NCBI36
NG_007110.2:g.82485del , LRG_218:g.82485del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2459-88del	ENSP00000495641.2:n.2459-88del
ENST00000233146.7:c.2459-88del MANE Select	ENSP00000233146.2:n.2459-88del
ENST00000543555.6:c.2261-88del	ENSP00000442697.1:n.2261-88del
ENST00000644092.1:c.*759-88del	ENSP00000496351.1:n.*759-88del
ENST00000644900.1:c.312-88del
ENST00000645339.1:c.2459-88del	ENSP00000496441.1:n.2459-88del
ENST00000645506.1:c.2459-88del	ENSP00000495455.1:n.2459-88del
ENST00000646415.1:c.2459-88del	ENSP00000495543.1:n.2459-88del
ENST00000233146.6:c.2459-88del	ENSP00000233146.2:n.2459-88del
ENST00000406134.5:c.2459-88del	ENSP00000384199.1:n.2459-88del
ENST00000543555.5:c.2261-88del	ENSP00000442697.1:n.2261-88del
ENST00000610696.4:c.*855-88del	ENSP00000483159.1:n.*855-88del
ENST00000613514.4:c.*999-88del	ENSP00000484137.1:n.*999-88del
ENST00000617333.3:c.*1225-88del	ENSP00000482468.1:n.*1225-88del
ENST00000617938.4:c.*1431-88del	ENSP00000481158.1:n.*1431-88del
ENST00000621359.2:c.*25-88del	ENSP00000481416.1:n.*25-88del
NM_000251.2:c.2459-88del , LRG_218t1:c.2459-88del	NP_000242.1:n.2459-88del
NM_001258281.1:c.2261-88del	NP_001245210.1:n.2261-88del
XM_005264332.2:c.2459-88del	XP_005264389.2:n.2459-88del
XM_011532867.1:c.2459-88del	XP_011531169.1:n.2459-88del
XR_939685.1:n.2531-88del
XM_005264332.4:c.2459-88del	XP_005264389.2:n.2459-88del
XM_011532867.2:c.2459-88del	XP_011531169.1:n.2459-88del
XR_001738747.2:n.2521-88del
XR_939685.2:n.2521-88del
NM_000251.3:c.2459-88del MANE Select	NP_000242.1:n.2459-88del