Canonical Allele Identifier: CA2082836240

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379460C= , CM000675.2:g.32379460C=	GRCh38
NC_000013.10:g.32953597C= , CM000675.1:g.32953597C=	GRCh37
NC_000013.9:g.31851597C=	NCBI36
NG_012772.3:g.68981C= , LRG_293:g.68981C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8898C=	ENSP00000434898.2:p.Val2966=
ENST00000528762.2:c.*265C=	ENSP00000433168.2:n.*265C=
ENST00000530893.7:c.8529C=	ENSP00000499438.2:p.Val2843=
ENST00000665585.2:c.*460C=	ENSP00000499570.2:n.*460C=
ENST00000666593.2:c.8898C=	ENSP00000499256.2:p.Val2966=
ENST00000700202.2:c.8898C=	ENSP00000514856.2:p.Val2966=
ENST00000700202.1:c.1365C=	ENSP00000514856.1:p.Val455=
ENST00000700203.1:n.1025C=
ENST00000380152.8:c.8898C= MANE Select	ENSP00000369497.3:p.Val2966=
ENST00000544455.6:c.8898C=	ENSP00000439902.1:p.Val2966=
ENST00000614259.2:c.8906C=	ENSP00000506251.1:n.8906C=
ENST00000665585.1:c.1776C=
ENST00000680887.1:c.8898C=	ENSP00000505508.1:p.Val2966=
ENST00000380152.7:c.8898C=	ENSP00000369497.3:p.Val2966=
ENST00000528762.1:c.460C=	ENSP00000433168.1:n.460C=
ENST00000544455.5:c.8898C=	ENSP00000439902.1:p.Val2966=
NM_000059.3:c.8898C= , LRG_293t1:c.8898C=	NP_000050.2:p.Val2966=
XM_011535203.1:c.8898C=	XP_011533505.1:p.Val2966=
XM_011535204.1:c.8802C=	XP_011533506.1:p.Val2934=
XM_011535205.1:c.8755-290C=	XP_011533507.1:n.8755-290C=
NM_000059.4:c.8898C= MANE Select	NP_000050.3:p.Val2966=