Canonical Allele Identifier: CA2082772506

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315523G= , CM000675.2:g.32315523G=	GRCh38
NC_000013.10:g.32889660G= , CM000675.1:g.32889660G=	GRCh37
NC_000013.9:g.31787660G=	NCBI36
NG_012772.3:g.5044G= , LRG_293:g.5044G=
NG_017006.1:g.1432C=
NG_017006.2:g.4841C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.-184G=	ENSP00000434898.2:n.-184G=
ENST00000528762.2:c.-184G=	ENSP00000433168.2:n.-184G=
ENST00000530893.7:c.-549G=	ENSP00000499438.2:n.-549G=
ENST00000665585.2:c.-184G=	ENSP00000499570.2:n.-184G=
ENST00000666593.2:c.-184G=	ENSP00000499256.2:n.-184G=
ENST00000700202.2:c.-184G=	ENSP00000514856.2:n.-184G=
ENST00000380152.8:c.-184G= MANE Select	ENSP00000369497.3:n.-184G=
ENST00000544455.6:c.-40+378G=	ENSP00000439902.1:n.-40+378G=
ENST00000380152.7:c.-184G=	ENSP00000369497.3:n.-184G=
ENST00000530893.6:n.19G=
ENST00000544455.5:c.-184G=	ENSP00000439902.1:n.-184G=
NM_000059.3:c.-184G= , LRG_293t1:c.-184G=	NP_000050.2:n.-184G=
XM_011535203.1:c.-40+378G=	XP_011533505.1:n.-40+378G=
XM_011535204.1:c.-184G=	XP_011533506.1:n.-184G=
XM_011535205.1:c.-184G=	XP_011533507.1:n.-184G=
NM_000059.4:c.-184G= MANE Select	NP_000050.3:n.-184G=