Canonical Allele Identifier: CA2082811023
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32337112_32337113delinsAC , CM000675.2:g.32337112_32337113delinsAC GRCh38
NC_000013.10:g.32911249_32911250delinsAC , CM000675.1:g.32911249_32911250delinsAC GRCh37
NC_000013.9:g.31809249_31809250delinsAC NCBI36
NG_012772.3:g.26633_26634delinsAC , LRG_293:g.26633_26634delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.2757_2758delinsAC ENSP00000434898.2:p.Glu919=
ENST00000528762.2:c.2757_2758delinsAC ENSP00000433168.2:p.Glu919=
ENST00000530893.7:c.2388_2389delinsAC ENSP00000499438.2:p.Glu796=
ENST00000665585.2:c.2757_2758delinsAC ENSP00000499570.2:p.Glu919=
ENST00000666593.2:c.2757_2758delinsAC ENSP00000499256.2:p.Glu919=
ENST00000700202.2:c.2757_2758delinsAC ENSP00000514856.2:p.Glu919=
ENST00000380152.8:c.2757_2758delinsAC MANE Select ENSP00000369497.3:p.Glu919=
ENST00000544455.6:c.2757_2758delinsAC ENSP00000439902.1:p.Glu919=
ENST00000614259.2:c.2757_2758delinsAC ENSP00000506251.1:p.Glu919=
ENST00000680887.1:c.2757_2758delinsAC ENSP00000505508.1:p.Glu919=
ENST00000380152.7:c.2757_2758delinsAC ENSP00000369497.3:p.Glu919=
ENST00000544455.5:c.2757_2758delinsAC ENSP00000439902.1:p.Glu919=
ENST00000614259.1:n.2757_2758delinsAC
NM_000059.3:c.2757_2758delinsAC , LRG_293t1:c.2757_2758delinsAC NP_000050.2:p.Glu919=
XM_011535203.1:c.2757_2758delinsAC XP_011533505.1:p.Glu919=
XM_011535204.1:c.2757_2758delinsAC XP_011533506.1:p.Glu919=
XM_011535205.1:c.2757_2758delinsAC XP_011533507.1:p.Glu919=
NM_000059.4:c.2757_2758delinsAC MANE Select NP_000050.3:p.Glu919=