Canonical Allele Identifier: CA1630855913

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32399302A= , CM000675.2:g.32399302A=	GRCh38
NC_000013.10:g.32973439A= , CM000675.1:g.32973439A=	GRCh37
NC_000013.9:g.31871439A=	NCBI36
NG_012772.3:g.88823A= , LRG_293:g.88823A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.*532A= MANE Select	NP_000050.3:n.*532A=
ENST00000380152.8:c.*532A= MANE Select	ENSP00000369497.3:n.*532A=
NM_000059.3:c.*532A= , LRG_293t1:c.*532A=	NP_000050.2:n.*532A=
ENST00000380152.7:c.*532A=	ENSP00000369497.3:n.*532A=
ENST00000470094.2:c.*1312A=	ENSP00000434898.2:n.*1312A=
ENST00000530893.7:c.*532A=	ENSP00000499438.2:n.*532A=
ENST00000544455.5:c.*440+92A=	ENSP00000439902.1:n.*440+92A=
ENST00000544455.6:c.*532A=	ENSP00000439902.1:n.*532A=
ENST00000614259.2:c.10797A=	ENSP00000506251.1:n.10797A=
ENST00000680887.1:c.*532A=	ENSP00000505508.1:n.*532A=
XM_011535203.1:c.*532A=	XP_011533505.1:n.*532A=
XM_011535204.1:c.*532A=	XP_011533506.1:n.*532A=