Canonical Allele Identifier: CA2082818795
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32357885_32357886delinsCA , CM000675.2:g.32357885_32357886delinsCA GRCh38
NC_000013.10:g.32932022_32932023delinsCA , CM000675.1:g.32932022_32932023delinsCA GRCh37
NC_000013.9:g.31830022_31830023delinsCA NCBI36
NG_012772.3:g.47406_47407delinsCA , LRG_293:g.47406_47407delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7761_7762delinsCA ENSP00000434898.2:p.Leu2587=
ENST00000528762.2:c.7761_7762delinsCA ENSP00000433168.2:p.Leu2587=
ENST00000530893.7:c.7392_7393delinsCA ENSP00000499438.2:p.Leu2464=
ENST00000665585.2:c.7761_7762delinsCA ENSP00000499570.2:p.Leu2587=
ENST00000666593.2:c.7761_7762delinsCA ENSP00000499256.2:p.Leu2587=
ENST00000700202.2:c.7761_7762delinsCA ENSP00000514856.2:p.Leu2587=
ENST00000700202.1:c.228_229delinsCA ENSP00000514856.1:p.Leu76=
ENST00000380152.8:c.7761_7762delinsCA MANE Select ENSP00000369497.3:p.Leu2587=
ENST00000544455.6:c.7761_7762delinsCA ENSP00000439902.1:p.Leu2587=
ENST00000614259.2:c.7761_7762delinsCA ENSP00000506251.1:p.Leu2587=
ENST00000665585.1:c.326_327delinsCA
ENST00000680887.1:c.7761_7762delinsCA ENSP00000505508.1:p.Leu2587=
ENST00000380152.7:c.7761_7762delinsCA ENSP00000369497.3:p.Leu2587=
ENST00000544455.5:c.7761_7762delinsCA ENSP00000439902.1:p.Leu2587=
ENST00000614259.1:n.7761_7762delinsCA
NM_000059.3:c.7761_7762delinsCA , LRG_293t1:c.7761_7762delinsCA NP_000050.2:p.Leu2587=
XM_011535203.1:c.7761_7762delinsCA XP_011533505.1:p.Leu2587=
XM_011535204.1:c.7665_7666delinsCA XP_011533506.1:p.Leu2555=
XM_011535205.1:c.7761_7762delinsCA XP_011533507.1:p.Leu2587=
NM_000059.4:c.7761_7762delinsCA MANE Select NP_000050.3:p.Leu2587=