Canonical Allele Identifier: CA2082835280

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398318A= , CM000675.2:g.32398318A=	GRCh38
NC_000013.10:g.32972455A= , CM000675.1:g.32972455A=	GRCh37
NC_000013.9:g.31870455A=	NCBI36
NG_012772.3:g.87839A= , LRG_293:g.87839A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*328A=	ENSP00000434898.2:n.*328A=
ENST00000528762.2:c.*1172A=	ENSP00000433168.2:n.*1172A=
ENST00000530893.7:c.9436A=	ENSP00000499438.2:p.Arg3146=
ENST00000665585.2:c.*1367A=	ENSP00000499570.2:n.*1367A=
ENST00000700202.2:c.9754A=	ENSP00000514856.2:p.Arg3252=
ENST00000700202.1:c.2221A=	ENSP00000514856.1:p.Arg741=
ENST00000700203.1:n.1932A=
ENST00000380152.8:c.9805A= MANE Select	ENSP00000369497.3:p.Arg3269=
ENST00000544455.6:c.9805A=	ENSP00000439902.1:p.Arg3269=
ENST00000614259.2:c.9813A=	ENSP00000506251.1:n.9813A=
ENST00000680887.1:c.9805A=	ENSP00000505508.1:p.Arg3269=
ENST00000380152.7:c.9805A=	ENSP00000369497.3:p.Arg3269=
ENST00000533776.1:n.393A=
ENST00000544455.5:c.9805A=	ENSP00000439902.1:p.Arg3269=
NM_000059.3:c.9805A= , LRG_293t1:c.9805A=	NP_000050.2:p.Arg3269=
XM_011535203.1:c.9805A=	XP_011533505.1:p.Arg3269=
XM_011535204.1:c.9709A=	XP_011533506.1:p.Arg3237=
NM_000059.4:c.9805A= MANE Select	NP_000050.3:p.Arg3269=