Canonical Allele Identifier: CA2082837731

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398664G= , CM000675.2:g.32398664G=	GRCh38
NC_000013.10:g.32972801G= , CM000675.1:g.32972801G=	GRCh37
NC_000013.9:g.31870801G=	NCBI36
NG_012772.3:g.88185G= , LRG_293:g.88185G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*674G=	ENSP00000434898.2:n.*674G=
ENST00000528762.2:c.*1518G=	ENSP00000433168.2:n.*1518G=
ENST00000530893.7:c.9782G=	ENSP00000499438.2:p.Arg3261=
ENST00000665585.2:c.*1713G=	ENSP00000499570.2:n.*1713G=
ENST00000700202.2:c.10100G=	ENSP00000514856.2:p.Arg3367=
ENST00000700202.1:c.2567G=	ENSP00000514856.1:p.Arg856=
ENST00000700203.1:n.2278G=
ENST00000380152.8:c.10151G= MANE Select	ENSP00000369497.3:p.Arg3384=
ENST00000544455.6:c.10151G=	ENSP00000439902.1:p.Arg3384=
ENST00000614259.2:c.10159G=	ENSP00000506251.1:n.10159G=
ENST00000680887.1:c.10151G=	ENSP00000505508.1:p.Arg3384=
ENST00000380152.7:c.10151G=	ENSP00000369497.3:p.Arg3384=
ENST00000544455.5:c.10151G=	ENSP00000439902.1:p.Arg3384=
NM_000059.3:c.10151G= , LRG_293t1:c.10151G=	NP_000050.2:p.Arg3384=
XM_011535203.1:c.10151G=	XP_011533505.1:p.Arg3384=
XM_011535204.1:c.10055G=	XP_011533506.1:p.Arg3352=
NM_000059.4:c.10151G= MANE Select	NP_000050.3:p.Arg3384=