Canonical Allele Identifier: CA2695217926

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32357886delinsTT , CM000675.2:g.32357886delinsTT	GRCh38
NC_000013.10:g.32932023delinsTT , CM000675.1:g.32932023delinsTT	GRCh37
NC_000013.9:g.31830023delinsTT	NCBI36
NG_012772.3:g.47407delinsTT , LRG_293:g.47407delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.7762delinsTT	ENSP00000434898.2:p.Ile2588PhefsTer5
ENST00000528762.2:c.7762delinsTT	ENSP00000433168.2:p.Ile2588PhefsTer5
ENST00000530893.7:c.7393delinsTT	ENSP00000499438.2:p.Ile2465PhefsTer5
ENST00000665585.2:c.7762delinsTT	ENSP00000499570.2:p.Ile2588PhefsTer5
ENST00000666593.2:c.7762delinsTT	ENSP00000499256.2:p.Ile2588PhefsTer5
ENST00000700202.2:c.7762delinsTT	ENSP00000514856.2:p.Ile2588PhefsTer5
ENST00000700202.1:c.229delinsTT	ENSP00000514856.1:p.Ile77PhefsTer5
ENST00000380152.8:c.7762delinsTT MANE Select	ENSP00000369497.3:p.Ile2588PhefsTer5
ENST00000544455.6:c.7762delinsTT	ENSP00000439902.1:p.Ile2588PhefsTer5
ENST00000614259.2:c.7762delinsTT	ENSP00000506251.1:p.Ile2588PhefsTer5
ENST00000665585.1:c.327delinsTT
ENST00000680887.1:c.7762delinsTT	ENSP00000505508.1:p.Ile2588PhefsTer5
ENST00000380152.7:c.7762delinsTT	ENSP00000369497.3:p.Ile2588PhefsTer5
ENST00000544455.5:c.7762delinsTT	ENSP00000439902.1:p.Ile2588PhefsTer5
ENST00000614259.1:n.7762delinsTT
NM_000059.3:c.7762delinsTT , LRG_293t1:c.7762delinsTT	NP_000050.2:p.Ile2588PhefsTer5
XM_011535203.1:c.7762delinsTT	XP_011533505.1:p.Ile2588PhefsTer5
XM_011535204.1:c.7666delinsTT	XP_011533506.1:p.Ile2556PhefsTer5
XM_011535205.1:c.7762delinsTT	XP_011533507.1:p.Ile2588PhefsTer5
NM_000059.4:c.7762delinsTT MANE Select	NP_000050.3:p.Ile2588PhefsTer5