Canonical Allele Identifier: CA2082835432

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398346C= , CM000675.2:g.32398346C=	GRCh38
NC_000013.10:g.32972483C= , CM000675.1:g.32972483C=	GRCh37
NC_000013.9:g.31870483C=	NCBI36
NG_012772.3:g.87867C= , LRG_293:g.87867C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*356C=	ENSP00000434898.2:n.*356C=
ENST00000528762.2:c.*1200C=	ENSP00000433168.2:n.*1200C=
ENST00000530893.7:c.9464C=	ENSP00000499438.2:p.Pro3155=
ENST00000665585.2:c.*1395C=	ENSP00000499570.2:n.*1395C=
ENST00000700202.2:c.9782C=	ENSP00000514856.2:p.Pro3261=
ENST00000700202.1:c.2249C=	ENSP00000514856.1:p.Pro750=
ENST00000700203.1:n.1960C=
ENST00000380152.8:c.9833C= MANE Select	ENSP00000369497.3:p.Pro3278=
ENST00000544455.6:c.9833C=	ENSP00000439902.1:p.Pro3278=
ENST00000614259.2:c.9841C=	ENSP00000506251.1:n.9841C=
ENST00000680887.1:c.9833C=	ENSP00000505508.1:p.Pro3278=
ENST00000380152.7:c.9833C=	ENSP00000369497.3:p.Pro3278=
ENST00000533776.1:n.421C=
ENST00000544455.5:c.9833C=	ENSP00000439902.1:p.Pro3278=
NM_000059.3:c.9833C= , LRG_293t1:c.9833C=	NP_000050.2:p.Pro3278=
XM_011535203.1:c.9833C=	XP_011533505.1:p.Pro3278=
XM_011535204.1:c.9737C=	XP_011533506.1:p.Pro3246=
NM_000059.4:c.9833C= MANE Select	NP_000050.3:p.Pro3278=