Canonical Allele Identifier: CA2495843696

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47429887_47429899delinsTATCAGGGTATAA , CM000664.2:g.47429887_47429899delinsTATCAGGGTATAA	GRCh38
NC_000002.11:g.47657026_47657038delinsTATCAGGGTATAA , CM000664.1:g.47657026_47657038delinsTATCAGGGTATAA	GRCh37
NC_000002.10:g.47510530_47510542delinsTATCAGGGTATAA	NCBI36
NG_007110.2:g.31764_31776delinsTATCAGGGTATAA , LRG_218:g.31764_31776delinsTATCAGGGTATAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.1222_1234delinsTATCAGGGTATAA	ENSP00000495641.2:p.Tyr408=
ENST00000233146.7:c.1222_1234delinsTATCAGGGTATAA MANE Select	ENSP00000233146.2:p.Tyr408=
ENST00000543555.6:c.1024_1036delinsTATCAGGGTATAA	ENSP00000442697.1:p.Tyr342=
ENST00000644092.1:c.1222_1234delinsTATCAGGGTATAA	ENSP00000496351.1:p.Tyr408=
ENST00000645339.1:c.1222_1234delinsTATCAGGGTATAA	ENSP00000496441.1:p.Tyr408=
ENST00000645506.1:c.1222_1234delinsTATCAGGGTATAA	ENSP00000495455.1:p.Tyr408=
ENST00000646415.1:c.1222_1234delinsTATCAGGGTATAA	ENSP00000495543.1:p.Tyr408=
ENST00000233146.6:c.1222_1234delinsTATCAGGGTATAA	ENSP00000233146.2:p.Tyr408=
ENST00000406134.5:c.1222_1234delinsTATCAGGGTATAA	ENSP00000384199.1:p.Tyr408=
ENST00000543555.5:c.1024_1036delinsTATCAGGGTATAA	ENSP00000442697.1:p.Tyr342=
ENST00000610696.4:c.1222_1234delinsTATCAGGGTATAA	ENSP00000483159.1:p.Tyr408=
ENST00000613514.4:c.1222_1234delinsTATCAGGGTATAA	ENSP00000484137.1:p.Tyr408=
ENST00000617333.3:c.1221_1233delinsTATCAGGGTATAA	ENSP00000482468.1:p.Ser407=
ENST00000617938.4:c.*194_*206delinsTATCAGGGTATAA	ENSP00000481158.1:n.*194_*206delinsTATCAG...
ENST00000621359.2:c.1222_1234delinsTATCAGGGTATAA	ENSP00000481416.1:p.Tyr408=
NM_000251.2:c.1222_1234delinsTATCAGGGTATAA , LRG_218t1:c.1222_1234delinsTATCAGGGTATAA	NP_000242.1:p.Tyr408=
NM_001258281.1:c.1024_1036delinsTATCAGGGTATAA	NP_001245210.1:p.Tyr342=
XM_005264332.2:c.1222_1234delinsTATCAGGGTATAA	XP_005264389.2:p.Tyr408=
XM_011532867.1:c.1222_1234delinsTATCAGGGTATAA	XP_011531169.1:p.Tyr408=
XR_939685.1:n.1294_1306delinsTATCAGGGTATAA
XM_005264332.4:c.1222_1234delinsTATCAGGGTATAA	XP_005264389.2:p.Tyr408=
XM_011532867.2:c.1222_1234delinsTATCAGGGTATAA	XP_011531169.1:p.Tyr408=
XR_001738747.2:n.1284_1296delinsTATCAGGGTATAA
XR_939685.2:n.1284_1296delinsTATCAGGGTATAA
NM_000251.3:c.1222_1234delinsTATCAGGGTATAA MANE Select	NP_000242.1:p.Tyr408=