Canonical Allele Identifier: CA026296

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32332456C>A , CM000675.2:g.32332456C>A	GRCh38
NC_000013.10:g.32906593C>A , CM000675.1:g.32906593C>A	GRCh37
NC_000013.9:g.31804593C>A	NCBI36
NG_012772.3:g.21977C>A , LRG_293:g.21977C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.978C>A	ENSP00000434898.2:p.Ser326Arg
ENST00000528762.2:c.978C>A	ENSP00000433168.2:p.Ser326Arg
ENST00000530893.7:c.609C>A	ENSP00000499438.2:p.Ser203Arg
ENST00000665585.2:c.978C>A	ENSP00000499570.2:p.Ser326Arg
ENST00000666593.2:c.978C>A	ENSP00000499256.2:p.Ser326Arg
ENST00000700202.2:c.978C>A	ENSP00000514856.2:p.Ser326Arg
ENST00000700201.1:c.*757C>A	ENSP00000514855.1:n.*757C>A
ENST00000380152.8:c.978C>A MANE Select	ENSP00000369497.3:p.Ser326Arg
ENST00000544455.6:c.978C>A	ENSP00000439902.1:p.Ser326Arg
ENST00000614259.2:c.978C>A	ENSP00000506251.1:p.Ser326Arg
ENST00000680887.1:c.978C>A	ENSP00000505508.1:p.Ser326Arg
ENST00000380152.7:c.978C>A	ENSP00000369497.3:p.Ser326Arg
ENST00000530893.6:n.1176C>A
ENST00000544455.5:c.978C>A	ENSP00000439902.1:p.Ser326Arg
ENST00000614259.1:n.978C>A
NM_000059.3:c.978C>A , LRG_293t1:c.978C>A	NP_000050.2:p.Ser326Arg
XM_011535203.1:c.978C>A	XP_011533505.1:p.Ser326Arg
XM_011535204.1:c.978C>A	XP_011533506.1:p.Ser326Arg
XM_011535205.1:c.978C>A	XP_011533507.1:p.Ser326Arg
NM_000059.4:c.978C>A MANE Select	NP_000050.3:p.Ser326Arg