Canonical Allele Identifier: CA2495834032

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414401_47414402delinsGC , CM000664.2:g.47414401_47414402delinsGC	GRCh38
NC_000002.11:g.47641540_47641541delinsGC , CM000664.1:g.47641540_47641541delinsGC	GRCh37
NC_000002.10:g.47495044_47495045delinsGC	NCBI36
NG_007110.2:g.16278_16279delinsGC , LRG_218:g.16278_16279delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.925_926delinsGC	ENSP00000495641.2:p.Ala309=
ENST00000233146.7:c.925_926delinsGC MANE Select	ENSP00000233146.2:p.Ala309=
ENST00000543555.6:c.727_728delinsGC	ENSP00000442697.1:p.Ala243=
ENST00000644092.1:c.925_926delinsGC	ENSP00000496351.1:p.Ala309=
ENST00000645339.1:c.925_926delinsGC	ENSP00000496441.1:p.Ala309=
ENST00000645506.1:c.925_926delinsGC	ENSP00000495455.1:p.Ala309=
ENST00000646415.1:c.925_926delinsGC	ENSP00000495543.1:p.Ala309=
ENST00000233146.6:c.925_926delinsGC	ENSP00000233146.2:p.Ala309=
ENST00000406134.5:c.925_926delinsGC	ENSP00000384199.1:p.Ala309=
ENST00000543555.5:c.727_728delinsGC	ENSP00000442697.1:p.Ala243=
ENST00000610696.4:c.925_926delinsGC	ENSP00000483159.1:p.Ala309=
ENST00000613514.4:c.925_926delinsGC	ENSP00000484137.1:p.Ala309=
ENST00000617333.3:c.925_926delinsGC	ENSP00000482468.1:p.Ala309=
ENST00000617938.4:c.925_926delinsGC	ENSP00000481158.1:p.Ala309=
ENST00000621359.2:c.925_926delinsGC	ENSP00000481416.1:p.Ala309=
NM_000251.2:c.925_926delinsGC , LRG_218t1:c.925_926delinsGC	NP_000242.1:p.Ala309=
NM_001258281.1:c.727_728delinsGC	NP_001245210.1:p.Ala243=
XM_005264332.2:c.925_926delinsGC	XP_005264389.2:p.Ala309=
XM_011532867.1:c.925_926delinsGC	XP_011531169.1:p.Ala309=
XR_939685.1:n.997_998delinsGC
XM_005264332.4:c.925_926delinsGC	XP_005264389.2:p.Ala309=
XM_011532867.2:c.925_926delinsGC	XP_011531169.1:p.Ala309=
XR_001738747.2:n.987_988delinsGC
XR_939685.2:n.987_988delinsGC
NM_000251.3:c.925_926delinsGC MANE Select	NP_000242.1:p.Ala309=