Canonical Allele Identifier: CA2586969089

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47408476_47408477delinsA , CM000664.2:g.47408476_47408477delinsA	GRCh38
NC_000002.11:g.47635615_47635616delinsA , CM000664.1:g.47635615_47635616delinsA	GRCh37
NC_000002.10:g.47489119_47489120delinsA	NCBI36
NG_007110.2:g.10353_10354delinsA , LRG_218:g.10353_10354delinsA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.287_288delinsA	ENSP00000495641.2:p.Arg96HisfsTer?
ENST00000233146.7:c.287_288delinsA MANE Select	ENSP00000233146.2:p.Arg96HisfsTer?
ENST00000543555.6:c.89_90delinsA	ENSP00000442697.1:p.Arg30HisfsTer?
ENST00000644092.1:c.287_288delinsA	ENSP00000496351.1:p.Arg96HisfsTer?
ENST00000645339.1:c.287_288delinsA	ENSP00000496441.1:p.Arg96HisfsTer?
ENST00000645506.1:c.287_288delinsA	ENSP00000495455.1:p.Arg96HisfsTer?
ENST00000646415.1:c.287_288delinsA	ENSP00000495543.1:p.Arg96HisfsTer?
ENST00000233146.6:c.287_288delinsA	ENSP00000233146.2:p.Arg96HisfsTer?
ENST00000406134.5:c.287_288delinsA	ENSP00000384199.1:p.Arg96HisfsTer?
ENST00000454849.5:c.89_90delinsA	ENSP00000411482.1:p.Arg30HisfsTer?
ENST00000543555.5:c.89_90delinsA	ENSP00000442697.1:p.Arg30HisfsTer?
ENST00000610696.4:c.287_288delinsA	ENSP00000483159.1:p.Arg96HisfsTer?
ENST00000613514.4:c.287_288delinsA	ENSP00000484137.1:p.Arg96HisfsTer?
ENST00000617333.3:c.287_288delinsA	ENSP00000482468.1:p.Arg96HisfsTer?
ENST00000617938.4:c.287_288delinsA	ENSP00000481158.1:p.Arg96HisfsTer?
ENST00000621359.2:c.287_288delinsA	ENSP00000481416.1:p.Arg96HisfsTer?
NM_000251.2:c.287_288delinsA , LRG_218t1:c.287_288delinsA	NP_000242.1:p.Arg96HisfsTer?
NM_001258281.1:c.89_90delinsA	NP_001245210.1:p.Arg30HisfsTer?
XM_005264332.2:c.287_288delinsA	XP_005264389.2:p.Arg96HisfsTer?
XM_011532867.1:c.287_288delinsA	XP_011531169.1:p.Arg96HisfsTer?
XR_939685.1:n.359_360delinsA
XM_005264332.4:c.287_288delinsA	XP_005264389.2:p.Arg96HisfsTer?
XM_011532867.2:c.287_288delinsA	XP_011531169.1:p.Arg96HisfsTer?
XR_001738747.2:n.349_350delinsA
XR_939685.2:n.349_350delinsA
NM_000251.3:c.287_288delinsA MANE Select	NP_000242.1:p.Arg96HisfsTer?