Canonical Allele Identifier: CA2082816540

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371093A= , CM000675.2:g.32371093A=	GRCh38
NC_000013.10:g.32945230A= , CM000675.1:g.32945230A=	GRCh37
NC_000013.9:g.31843230A=	NCBI36
NG_012772.3:g.60614A= , LRG_293:g.60614A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8625A=	ENSP00000434898.2:p.Glu2875=
ENST00000528762.2:c.8625A=	ENSP00000433168.2:p.Glu2875=
ENST00000530893.7:c.8256A=	ENSP00000499438.2:p.Glu2752=
ENST00000665585.2:c.8625A=	ENSP00000499570.2:p.Glu2875=
ENST00000666593.2:c.8625A=	ENSP00000499256.2:p.Glu2875=
ENST00000700202.2:c.8625A=	ENSP00000514856.2:p.Glu2875=
ENST00000700202.1:c.1092A=	ENSP00000514856.1:p.Glu364=
ENST00000380152.8:c.8625A= MANE Select	ENSP00000369497.3:p.Glu2875=
ENST00000544455.6:c.8625A=	ENSP00000439902.1:p.Glu2875=
ENST00000614259.2:c.8633A=	ENSP00000506251.1:n.8633A=
ENST00000665585.1:c.1190A=
ENST00000680887.1:c.8625A=	ENSP00000505508.1:p.Glu2875=
ENST00000380152.7:c.8625A=	ENSP00000369497.3:p.Glu2875=
ENST00000528762.1:c.123A=	ENSP00000433168.1:p.Glu41=
ENST00000544455.5:c.8625A=	ENSP00000439902.1:p.Glu2875=
NM_000059.3:c.8625A= , LRG_293t1:c.8625A=	NP_000050.2:p.Glu2875=
XM_011535203.1:c.8625A=	XP_011533505.1:p.Glu2875=
XM_011535204.1:c.8529A=	XP_011533506.1:p.Glu2843=
XM_011535205.1:c.8625A=	XP_011533507.1:p.Glu2875=
NM_000059.4:c.8625A= MANE Select	NP_000050.3:p.Glu2875=