Canonical Allele Identifier: CA2082759730

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32331015G= , CM000675.2:g.32331015G=	GRCh38
NC_000013.10:g.32905152G= , CM000675.1:g.32905152G=	GRCh37
NC_000013.9:g.31803152G=	NCBI36
NG_012772.3:g.20536G= , LRG_293:g.20536G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.778G=	ENSP00000434898.2:p.Glu260=
ENST00000528762.2:c.778G=	ENSP00000433168.2:p.Glu260=
ENST00000530893.7:c.409G=	ENSP00000499438.2:p.Glu137=
ENST00000665585.2:c.778G=	ENSP00000499570.2:p.Glu260=
ENST00000666593.2:c.778G=	ENSP00000499256.2:p.Glu260=
ENST00000700202.2:c.778G=	ENSP00000514856.2:p.Glu260=
ENST00000700201.1:c.*557G=	ENSP00000514855.1:n.*557G=
ENST00000380152.8:c.778G= MANE Select	ENSP00000369497.3:p.Glu260=
ENST00000544455.6:c.778G=	ENSP00000439902.1:p.Glu260=
ENST00000614259.2:c.778G=	ENSP00000506251.1:p.Glu260=
ENST00000680887.1:c.778G=	ENSP00000505508.1:p.Glu260=
ENST00000380152.7:c.778G=	ENSP00000369497.3:p.Glu260=
ENST00000530893.6:n.976G=
ENST00000544455.5:c.778G=	ENSP00000439902.1:p.Glu260=
ENST00000614259.1:n.778G=
NM_000059.3:c.778G= , LRG_293t1:c.778G=	NP_000050.2:p.Glu260=
XM_011535203.1:c.778G=	XP_011533505.1:p.Glu260=
XM_011535204.1:c.778G=	XP_011533506.1:p.Glu260=
XM_011535205.1:c.778G=	XP_011533507.1:p.Glu260=
NM_000059.4:c.778G= MANE Select	NP_000050.3:p.Glu260=