Canonical Allele Identifier: CA46683885

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414287_47414290delinsGTCT , CM000664.2:g.47414287_47414290delinsGTCT	GRCh38
NC_000002.11:g.47641426_47641429delinsGTCT , CM000664.1:g.47641426_47641429delinsGTCT	GRCh37
NC_000002.10:g.47494930_47494933delinsGTCT	NCBI36
NG_007110.2:g.16164_16167delinsGTCT , LRG_218:g.16164_16167delinsGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.811_814delinsGTCT	ENSP00000495641.2:p.Ser271_Ala272delinsValSer
ENST00000233146.7:c.811_814delinsGTCT MANE Select	ENSP00000233146.2:p.Ser271_Ala272delinsValSer
ENST00000543555.6:c.613_616delinsGTCT	ENSP00000442697.1:p.Ser205_Ala206delinsValSer
ENST00000644092.1:c.811_814delinsGTCT	ENSP00000496351.1:p.Ser271_Ala272delinsValSer
ENST00000645339.1:c.811_814delinsGTCT	ENSP00000496441.1:p.Ser271_Ala272delinsValSer
ENST00000645506.1:c.811_814delinsGTCT	ENSP00000495455.1:p.Ser271_Ala272delinsValSer
ENST00000646415.1:c.811_814delinsGTCT	ENSP00000495543.1:p.Ser271_Ala272delinsValSer
ENST00000233146.6:c.811_814delinsGTCT	ENSP00000233146.2:p.Ser271_Ala272delinsValSer
ENST00000406134.5:c.811_814delinsGTCT	ENSP00000384199.1:p.Ser271_Ala272delinsValSer
ENST00000543555.5:c.613_616delinsGTCT	ENSP00000442697.1:p.Ser205_Ala206delinsValSer
ENST00000610696.4:c.811_814delinsGTCT	ENSP00000483159.1:p.Ser271_Ala272delinsValSer
ENST00000613514.4:c.811_814delinsGTCT	ENSP00000484137.1:p.Ser271_Ala272delinsValSer
ENST00000617333.3:c.811_814delinsGTCT	ENSP00000482468.1:p.Ser271_Ala272delinsValSer
ENST00000617938.4:c.811_814delinsGTCT	ENSP00000481158.1:p.Ser271_Ala272delinsValSer
ENST00000621359.2:c.811_814delinsGTCT	ENSP00000481416.1:p.Ser271_Ala272delinsValSer
NM_000251.2:c.811_814delinsGTCT , LRG_218t1:c.811_814delinsGTCT	NP_000242.1:p.Ser271_Ala272delinsValSer
NM_001258281.1:c.613_616delinsGTCT	NP_001245210.1:p.Ser205_Ala206delinsValSer
XM_005264332.2:c.811_814delinsGTCT	XP_005264389.2:p.Ser271_Ala272delinsValSer
XM_011532867.1:c.811_814delinsGTCT	XP_011531169.1:p.Ser271_Ala272delinsValSer
XR_939685.1:n.883_886delinsGTCT
XM_005264332.4:c.811_814delinsGTCT	XP_005264389.2:p.Ser271_Ala272delinsValSer
XM_011532867.2:c.811_814delinsGTCT	XP_011531169.1:p.Ser271_Ala272delinsValSer
XR_001738747.2:n.873_876delinsGTCT
XR_939685.2:n.873_876delinsGTCT
NM_000251.3:c.811_814delinsGTCT MANE Select	NP_000242.1:p.Ser271_Ala272delinsValSer