Canonical Allele Identifier: CA2082811387

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32337149_32337151delinsGAC , CM000675.2:g.32337149_32337151delinsGAC	GRCh38
NC_000013.10:g.32911286_32911288delinsGAC , CM000675.1:g.32911286_32911288delinsGAC	GRCh37
NC_000013.9:g.31809286_31809288delinsGAC	NCBI36
NG_012772.3:g.26670_26672delinsGAC , LRG_293:g.26670_26672delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.2794_2796delinsGAC	ENSP00000434898.2:p.Asp932=
ENST00000528762.2:c.2794_2796delinsGAC	ENSP00000433168.2:p.Asp932=
ENST00000530893.7:c.2425_2427delinsGAC	ENSP00000499438.2:p.Asp809=
ENST00000665585.2:c.2794_2796delinsGAC	ENSP00000499570.2:p.Asp932=
ENST00000666593.2:c.2794_2796delinsGAC	ENSP00000499256.2:p.Asp932=
ENST00000700202.2:c.2794_2796delinsGAC	ENSP00000514856.2:p.Asp932=
ENST00000380152.8:c.2794_2796delinsGAC MANE Select	ENSP00000369497.3:p.Asp932=
ENST00000544455.6:c.2794_2796delinsGAC	ENSP00000439902.1:p.Asp932=
ENST00000614259.2:c.2794_2796delinsGAC	ENSP00000506251.1:p.Asp932=
ENST00000680887.1:c.2794_2796delinsGAC	ENSP00000505508.1:p.Asp932=
ENST00000380152.7:c.2794_2796delinsGAC	ENSP00000369497.3:p.Asp932=
ENST00000544455.5:c.2794_2796delinsGAC	ENSP00000439902.1:p.Asp932=
ENST00000614259.1:n.2794_2796delinsGAC
NM_000059.3:c.2794_2796delinsGAC , LRG_293t1:c.2794_2796delinsGAC	NP_000050.2:p.Asp932=
XM_011535203.1:c.2794_2796delinsGAC	XP_011533505.1:p.Asp932=
XM_011535204.1:c.2794_2796delinsGAC	XP_011533506.1:p.Asp932=
XM_011535205.1:c.2794_2796delinsGAC	XP_011533507.1:p.Asp932=
NM_000059.4:c.2794_2796delinsGAC MANE Select	NP_000050.3:p.Asp932=