Canonical Allele Identifier: CA2495875994

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480676_47480677delinsCT , CM000664.2:g.47480676_47480677delinsCT	GRCh38
NC_000002.11:g.47707815_47707816delinsCT , CM000664.1:g.47707815_47707816delinsCT	GRCh37
NC_000002.10:g.47561319_47561320delinsCT	NCBI36
NG_007110.2:g.82553_82554delinsCT , LRG_218:g.82553_82554delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2459-20_2459-19delinsCT	ENSP00000495641.2:n.2459-20_2459-19delinsCT
ENST00000233146.7:c.2459-20_2459-19delinsCT MANE Select	ENSP00000233146.2:n.2459-20_2459-19delinsCT
ENST00000543555.6:c.2261-20_2261-19delinsCT	ENSP00000442697.1:n.2261-20_2261-19delinsCT
ENST00000644092.1:c.*759-20_*759-19delinsCT	ENSP00000496351.1:n.*759-20_*759-19delinsCT
ENST00000644900.1:c.312-20_312-19delinsCT
ENST00000645339.1:c.2459-20_2459-19delinsCT	ENSP00000496441.1:n.2459-20_2459-19delinsCT
ENST00000645506.1:c.2459-20_2459-19delinsCT	ENSP00000495455.1:n.2459-20_2459-19delinsCT
ENST00000646415.1:c.2459-20_2459-19delinsCT	ENSP00000495543.1:n.2459-20_2459-19delinsCT
ENST00000233146.6:c.2459-20_2459-19delinsCT	ENSP00000233146.2:n.2459-20_2459-19delinsCT
ENST00000406134.5:c.2459-20_2459-19delinsCT	ENSP00000384199.1:n.2459-20_2459-19delinsCT
ENST00000543555.5:c.2261-20_2261-19delinsCT	ENSP00000442697.1:n.2261-20_2261-19delinsCT
ENST00000610696.4:c.*855-20_*855-19delinsCT	ENSP00000483159.1:n.*855-20_*855-19delinsCT
ENST00000613514.4:c.*999-20_*999-19delinsCT	ENSP00000484137.1:n.*999-20_*999-19delinsCT
ENST00000617333.3:c.*1225-20_*1225-19delinsCT	ENSP00000482468.1:n.*1225-20_*1225-19delinsCT
ENST00000617938.4:c.*1431-20_*1431-19delinsCT	ENSP00000481158.1:n.*1431-20_*1431-19delinsCT
ENST00000621359.2:c.*25-20_*25-19delinsCT	ENSP00000481416.1:n.*25-20_*25-19delinsCT
NM_000251.2:c.2459-20_2459-19delinsCT , LRG_218t1:c.2459-20_2459-19delinsCT	NP_000242.1:n.2459-20_2459-19delinsCT
NM_001258281.1:c.2261-20_2261-19delinsCT	NP_001245210.1:n.2261-20_2261-19delinsCT
XM_005264332.2:c.2459-20_2459-19delinsCT	XP_005264389.2:n.2459-20_2459-19delinsCT
XM_011532867.1:c.2459-20_2459-19delinsCT	XP_011531169.1:n.2459-20_2459-19delinsCT
XR_939685.1:n.2531-20_2531-19delinsCT
XM_005264332.4:c.2459-20_2459-19delinsCT	XP_005264389.2:n.2459-20_2459-19delinsCT
XM_011532867.2:c.2459-20_2459-19delinsCT	XP_011531169.1:n.2459-20_2459-19delinsCT
XR_001738747.2:n.2521-20_2521-19delinsCT
XR_939685.2:n.2521-20_2521-19delinsCT
NM_000251.3:c.2459-20_2459-19delinsCT MANE Select	NP_000242.1:n.2459-20_2459-19delinsCT