Canonical Allele Identifier: CA2082836776

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398564G= , CM000675.2:g.32398564G=	GRCh38
NC_000013.10:g.32972701G= , CM000675.1:g.32972701G=	GRCh37
NC_000013.9:g.31870701G=	NCBI36
NG_012772.3:g.88085G= , LRG_293:g.88085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*574G=	ENSP00000434898.2:n.*574G=
ENST00000528762.2:c.*1418G=	ENSP00000433168.2:n.*1418G=
ENST00000530893.7:c.9682G=	ENSP00000499438.2:p.Ala3228=
ENST00000665585.2:c.*1613G=	ENSP00000499570.2:n.*1613G=
ENST00000700202.2:c.10000G=	ENSP00000514856.2:p.Ala3334=
ENST00000700202.1:c.2467G=	ENSP00000514856.1:p.Ala823=
ENST00000700203.1:n.2178G=
ENST00000380152.8:c.10051G= MANE Select	ENSP00000369497.3:p.Ala3351=
ENST00000544455.6:c.10051G=	ENSP00000439902.1:p.Ala3351=
ENST00000614259.2:c.10059G=	ENSP00000506251.1:n.10059G=
ENST00000680887.1:c.10051G=	ENSP00000505508.1:p.Ala3351=
ENST00000380152.7:c.10051G=	ENSP00000369497.3:p.Ala3351=
ENST00000544455.5:c.10051G=	ENSP00000439902.1:p.Ala3351=
NM_000059.3:c.10051G= , LRG_293t1:c.10051G=	NP_000050.2:p.Ala3351=
XM_011535203.1:c.10051G=	XP_011533505.1:p.Ala3351=
XM_011535204.1:c.9955G=	XP_011533506.1:p.Ala3319=
NM_000059.4:c.10051G= MANE Select	NP_000050.3:p.Ala3351=