Canonical Allele Identifier: CA2082772708

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315568G= , CM000675.2:g.32315568G=	GRCh38
NC_000013.10:g.32889705G= , CM000675.1:g.32889705G=	GRCh37
NC_000013.9:g.31787705G=	NCBI36
NG_012772.3:g.5089G= , LRG_293:g.5089G=
NG_017006.1:g.1387C=
NG_017006.2:g.4796C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.-139G=	ENSP00000434898.2:n.-139G=
ENST00000528762.2:c.-139G=	ENSP00000433168.2:n.-139G=
ENST00000530893.7:c.-504G=	ENSP00000499438.2:n.-504G=
ENST00000665585.2:c.-139G=	ENSP00000499570.2:n.-139G=
ENST00000666593.2:c.-139G=	ENSP00000499256.2:n.-139G=
ENST00000700202.2:c.-139G=	ENSP00000514856.2:n.-139G=
ENST00000380152.8:c.-139G= MANE Select	ENSP00000369497.3:n.-139G=
ENST00000544455.6:c.-40+423G=	ENSP00000439902.1:n.-40+423G=
ENST00000380152.7:c.-139G=	ENSP00000369497.3:n.-139G=
ENST00000530893.6:n.64G=
ENST00000544455.5:c.-139G=	ENSP00000439902.1:n.-139G=
NM_000059.3:c.-139G= , LRG_293t1:c.-139G=	NP_000050.2:n.-139G=
XM_011535203.1:c.-40+423G=	XP_011533505.1:n.-40+423G=
XM_011535204.1:c.-139G=	XP_011533506.1:n.-139G=
XM_011535205.1:c.-139G=	XP_011533507.1:n.-139G=
NM_000059.4:c.-139G= MANE Select	NP_000050.3:n.-139G=