Canonical Allele Identifier: CA2082837677

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398656A= , CM000675.2:g.32398656A=	GRCh38
NC_000013.10:g.32972793A= , CM000675.1:g.32972793A=	GRCh37
NC_000013.9:g.31870793A=	NCBI36
NG_012772.3:g.88177A= , LRG_293:g.88177A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*666A=	ENSP00000434898.2:n.*666A=
ENST00000528762.2:c.*1510A=	ENSP00000433168.2:n.*1510A=
ENST00000530893.7:c.9774A=	ENSP00000499438.2:p.Arg3258=
ENST00000665585.2:c.*1705A=	ENSP00000499570.2:n.*1705A=
ENST00000700202.2:c.10092A=	ENSP00000514856.2:p.Arg3364=
ENST00000700202.1:c.2559A=	ENSP00000514856.1:p.Arg853=
ENST00000700203.1:n.2270A=
ENST00000380152.8:c.10143A= MANE Select	ENSP00000369497.3:p.Arg3381=
ENST00000544455.6:c.10143A=	ENSP00000439902.1:p.Arg3381=
ENST00000614259.2:c.10151A=	ENSP00000506251.1:n.10151A=
ENST00000680887.1:c.10143A=	ENSP00000505508.1:p.Arg3381=
ENST00000380152.7:c.10143A=	ENSP00000369497.3:p.Arg3381=
ENST00000544455.5:c.10143A=	ENSP00000439902.1:p.Arg3381=
NM_000059.3:c.10143A= , LRG_293t1:c.10143A=	NP_000050.2:p.Arg3381=
XM_011535203.1:c.10143A=	XP_011533505.1:p.Arg3381=
XM_011535204.1:c.10047A=	XP_011533506.1:p.Arg3349=
NM_000059.4:c.10143A= MANE Select	NP_000050.3:p.Arg3381=