Canonical Allele Identifier: CA2495873426

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47476391_47476393delinsCAT , CM000664.2:g.47476391_47476393delinsCAT	GRCh38
NC_000002.11:g.47703530_47703532delinsCAT , CM000664.1:g.47703530_47703532delinsCAT	GRCh37
NC_000002.10:g.47557034_47557036delinsCAT	NCBI36
NG_007110.2:g.78268_78270delinsCAT , LRG_218:g.78268_78270delinsCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.2030_2032delinsCAT	ENSP00000495641.2:p.Thr677=
ENST00000233146.7:c.2030_2032delinsCAT MANE Select	ENSP00000233146.2:p.Thr677=
ENST00000543555.6:c.1832_1834delinsCAT	ENSP00000442697.1:p.Thr611=
ENST00000644092.1:c.*330_*332delinsCAT	ENSP00000496351.1:n.*330_*332delinsCAT
ENST00000645339.1:c.2030_2032delinsCAT	ENSP00000496441.1:p.Thr677=
ENST00000645506.1:c.2030_2032delinsCAT	ENSP00000495455.1:p.Thr677=
ENST00000646415.1:c.2030_2032delinsCAT	ENSP00000495543.1:p.Thr677=
ENST00000233146.6:c.2030_2032delinsCAT	ENSP00000233146.2:p.Thr677=
ENST00000406134.5:c.2030_2032delinsCAT	ENSP00000384199.1:p.Thr677=
ENST00000543555.5:c.1832_1834delinsCAT	ENSP00000442697.1:p.Thr611=
ENST00000610696.4:c.*426_*428delinsCAT	ENSP00000483159.1:n.*426_*428delinsCAT
ENST00000613514.4:c.*570_*572delinsCAT	ENSP00000484137.1:n.*570_*572delinsCAT
ENST00000617333.3:c.*796_*798delinsCAT	ENSP00000482468.1:n.*796_*798delinsCAT
ENST00000617938.4:c.*1002_*1004delinsCAT	ENSP00000481158.1:n.*1002_*1004delinsCAT
ENST00000621359.2:c.2030_2032delinsCAT	ENSP00000481416.1:p.Thr677=
NM_000251.2:c.2030_2032delinsCAT , LRG_218t1:c.2030_2032delinsCAT	NP_000242.1:p.Thr677=
NM_001258281.1:c.1832_1834delinsCAT	NP_001245210.1:p.Thr611=
XM_005264332.2:c.2030_2032delinsCAT	XP_005264389.2:p.Thr677=
XM_011532867.1:c.2030_2032delinsCAT	XP_011531169.1:p.Thr677=
XR_939685.1:n.2102_2104delinsCAT
XM_005264332.4:c.2030_2032delinsCAT	XP_005264389.2:p.Thr677=
XM_011532867.2:c.2030_2032delinsCAT	XP_011531169.1:p.Thr677=
XR_001738747.2:n.2092_2094delinsCAT
XR_939685.2:n.2092_2094delinsCAT
NM_000251.3:c.2030_2032delinsCAT MANE Select	NP_000242.1:p.Thr677=