Canonical Allele Identifier: CA2082834853

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398266G= , CM000675.2:g.32398266G=	GRCh38
NC_000013.10:g.32972403G= , CM000675.1:g.32972403G=	GRCh37
NC_000013.9:g.31870403G=	NCBI36
NG_012772.3:g.87787G= , LRG_293:g.87787G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*276G=	ENSP00000434898.2:n.*276G=
ENST00000528762.2:c.*1120G=	ENSP00000433168.2:n.*1120G=
ENST00000530893.7:c.9384G=	ENSP00000499438.2:p.Lys3128=
ENST00000665585.2:c.*1315G=	ENSP00000499570.2:n.*1315G=
ENST00000700202.2:c.9702G=	ENSP00000514856.2:p.Lys3234=
ENST00000700202.1:c.2169G=	ENSP00000514856.1:p.Lys723=
ENST00000700203.1:n.1880G=
ENST00000380152.8:c.9753G= MANE Select	ENSP00000369497.3:p.Lys3251=
ENST00000544455.6:c.9753G=	ENSP00000439902.1:p.Lys3251=
ENST00000614259.2:c.9761G=	ENSP00000506251.1:n.9761G=
ENST00000680887.1:c.9753G=	ENSP00000505508.1:p.Lys3251=
ENST00000380152.7:c.9753G=	ENSP00000369497.3:p.Lys3251=
ENST00000470094.1:c.836G=
ENST00000533776.1:n.341G=
ENST00000544455.5:c.9753G=	ENSP00000439902.1:p.Lys3251=
NM_000059.3:c.9753G= , LRG_293t1:c.9753G=	NP_000050.2:p.Lys3251=
XM_011535203.1:c.9753G=	XP_011533505.1:p.Lys3251=
XM_011535204.1:c.9657G=	XP_011533506.1:p.Lys3219=
NM_000059.4:c.9753G= MANE Select	NP_000050.3:p.Lys3251=