Canonical Allele Identifier: CA2082832336

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362693G= , CM000675.2:g.32362693G=	GRCh38
NC_000013.10:g.32936830G= , CM000675.1:g.32936830G=	GRCh37
NC_000013.9:g.31834830G=	NCBI36
NG_012772.3:g.52214G= , LRG_293:g.52214G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.7976G=	ENSP00000434898.2:p.Arg2659=
ENST00000528762.2:c.7976G=	ENSP00000433168.2:p.Arg2659=
ENST00000530893.7:c.7607G=	ENSP00000499438.2:p.Arg2536=
ENST00000665585.2:c.7976G=	ENSP00000499570.2:p.Arg2659=
ENST00000666593.2:c.7976G=	ENSP00000499256.2:p.Arg2659=
ENST00000700202.2:c.7976G=	ENSP00000514856.2:p.Arg2659=
ENST00000700202.1:c.443G=	ENSP00000514856.1:p.Arg148=
ENST00000380152.8:c.7976G= MANE Select	ENSP00000369497.3:p.Arg2659=
ENST00000544455.6:c.7976G=	ENSP00000439902.1:p.Arg2659=
ENST00000614259.2:c.7984G=	ENSP00000506251.1:n.7984G=
ENST00000665585.1:c.541G=
ENST00000680887.1:c.7976G=	ENSP00000505508.1:p.Arg2659=
ENST00000380152.7:c.7976G=	ENSP00000369497.3:p.Arg2659=
ENST00000544455.5:c.7976G=	ENSP00000439902.1:p.Arg2659=
NM_000059.3:c.7976G= , LRG_293t1:c.7976G=	NP_000050.2:p.Arg2659=
XM_011535203.1:c.7976G=	XP_011533505.1:p.Arg2659=
XM_011535204.1:c.7880G=	XP_011533506.1:p.Arg2627=
XM_011535205.1:c.7976G=	XP_011533507.1:p.Arg2659=
NM_000059.4:c.7976G= MANE Select	NP_000050.3:p.Arg2659=