Canonical Allele Identifier: CA2495872463

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475116_47475117delinsTC , CM000664.2:g.47475116_47475117delinsTC	GRCh38
NC_000002.11:g.47702255_47702256delinsTC , CM000664.1:g.47702255_47702256delinsTC	GRCh37
NC_000002.10:g.47555759_47555760delinsTC	NCBI36
NG_007110.2:g.76993_76994delinsTC , LRG_218:g.76993_76994delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1851_1852delinsTC	ENSP00000495641.2:p.Val617=
ENST00000233146.7:c.1851_1852delinsTC MANE Select	ENSP00000233146.2:p.Val617=
ENST00000543555.6:c.1653_1654delinsTC	ENSP00000442697.1:p.Val551=
ENST00000644092.1:c.*151_*152delinsTC	ENSP00000496351.1:n.*151_*152delinsTC
ENST00000645339.1:c.1851_1852delinsTC	ENSP00000496441.1:p.Val617=
ENST00000645506.1:c.1851_1852delinsTC	ENSP00000495455.1:p.Val617=
ENST00000646415.1:c.1851_1852delinsTC	ENSP00000495543.1:p.Val617=
ENST00000233146.6:c.1851_1852delinsTC	ENSP00000233146.2:p.Val617=
ENST00000406134.5:c.1851_1852delinsTC	ENSP00000384199.1:p.Val617=
ENST00000543555.5:c.1653_1654delinsTC	ENSP00000442697.1:p.Val551=
ENST00000610696.4:c.*247_*248delinsTC	ENSP00000483159.1:n.*247_*248delinsTC
ENST00000613514.4:c.*391_*392delinsTC	ENSP00000484137.1:n.*391_*392delinsTC
ENST00000617333.3:c.*617_*618delinsTC	ENSP00000482468.1:n.*617_*618delinsTC
ENST00000617938.4:c.*823_*824delinsTC	ENSP00000481158.1:n.*823_*824delinsTC
ENST00000621359.2:c.1851_1852delinsTC	ENSP00000481416.1:p.Val617=
NM_000251.2:c.1851_1852delinsTC , LRG_218t1:c.1851_1852delinsTC	NP_000242.1:p.Val617=
NM_001258281.1:c.1653_1654delinsTC	NP_001245210.1:p.Val551=
XM_005264332.2:c.1851_1852delinsTC	XP_005264389.2:p.Val617=
XM_011532867.1:c.1851_1852delinsTC	XP_011531169.1:p.Val617=
XR_939685.1:n.1923_1924delinsTC
XM_005264332.4:c.1851_1852delinsTC	XP_005264389.2:p.Val617=
XM_011532867.2:c.1851_1852delinsTC	XP_011531169.1:p.Val617=
XR_001738747.2:n.1913_1914delinsTC
XR_939685.2:n.1913_1914delinsTC
NM_000251.3:c.1851_1852delinsTC MANE Select	NP_000242.1:p.Val617=