Canonical Allele Identifier: CA2495872602

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475268_47475269delinsCT , CM000664.2:g.47475268_47475269delinsCT	GRCh38
NC_000002.11:g.47702407_47702408delinsCT , CM000664.1:g.47702407_47702408delinsCT	GRCh37
NC_000002.10:g.47555911_47555912delinsCT	NCBI36
NG_007110.2:g.77145_77146delinsCT , LRG_218:g.77145_77146delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2003_2004delinsCT	ENSP00000495641.2:p.Thr668=
ENST00000233146.7:c.2003_2004delinsCT MANE Select	ENSP00000233146.2:p.Thr668=
ENST00000543555.6:c.1805_1806delinsCT	ENSP00000442697.1:p.Thr602=
ENST00000644092.1:c.*303_*304delinsCT	ENSP00000496351.1:n.*303_*304delinsCT
ENST00000645339.1:c.2003_2004delinsCT	ENSP00000496441.1:p.Thr668=
ENST00000645506.1:c.2003_2004delinsCT	ENSP00000495455.1:p.Thr668=
ENST00000646415.1:c.2003_2004delinsCT	ENSP00000495543.1:p.Thr668=
ENST00000233146.6:c.2003_2004delinsCT	ENSP00000233146.2:p.Thr668=
ENST00000406134.5:c.2003_2004delinsCT	ENSP00000384199.1:p.Thr668=
ENST00000543555.5:c.1805_1806delinsCT	ENSP00000442697.1:p.Thr602=
ENST00000610696.4:c.*399_*400delinsCT	ENSP00000483159.1:n.*399_*400delinsCT
ENST00000613514.4:c.*543_*544delinsCT	ENSP00000484137.1:n.*543_*544delinsCT
ENST00000617333.3:c.*769_*770delinsCT	ENSP00000482468.1:n.*769_*770delinsCT
ENST00000617938.4:c.*975_*976delinsCT	ENSP00000481158.1:n.*975_*976delinsCT
ENST00000621359.2:c.2003_2004delinsCT	ENSP00000481416.1:p.Thr668=
NM_000251.2:c.2003_2004delinsCT , LRG_218t1:c.2003_2004delinsCT	NP_000242.1:p.Thr668=
NM_001258281.1:c.1805_1806delinsCT	NP_001245210.1:p.Thr602=
XM_005264332.2:c.2003_2004delinsCT	XP_005264389.2:p.Thr668=
XM_011532867.1:c.2003_2004delinsCT	XP_011531169.1:p.Thr668=
XR_939685.1:n.2075_2076delinsCT
XM_005264332.4:c.2003_2004delinsCT	XP_005264389.2:p.Thr668=
XM_011532867.2:c.2003_2004delinsCT	XP_011531169.1:p.Thr668=
XR_001738747.2:n.2065_2066delinsCT
XR_939685.2:n.2065_2066delinsCT
NM_000251.3:c.2003_2004delinsCT MANE Select	NP_000242.1:p.Thr668=