Canonical Allele Identifier: CA2082834243

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398211G= , CM000675.2:g.32398211G=	GRCh38
NC_000013.10:g.32972348G= , CM000675.1:g.32972348G=	GRCh37
NC_000013.9:g.31870348G=	NCBI36
NG_012772.3:g.87732G= , LRG_293:g.87732G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*221G=	ENSP00000434898.2:n.*221G=
ENST00000528762.2:c.*1065G=	ENSP00000433168.2:n.*1065G=
ENST00000530893.7:c.9329G=	ENSP00000499438.2:p.Cys3110=
ENST00000665585.2:c.*1260G=	ENSP00000499570.2:n.*1260G=
ENST00000700202.2:c.9647G=	ENSP00000514856.2:p.Cys3216=
ENST00000700202.1:c.2114G=	ENSP00000514856.1:p.Cys705=
ENST00000700203.1:n.1825G=
ENST00000380152.8:c.9698G= MANE Select	ENSP00000369497.3:p.Cys3233=
ENST00000544455.6:c.9698G=	ENSP00000439902.1:p.Cys3233=
ENST00000614259.2:c.9706G=	ENSP00000506251.1:n.9706G=
ENST00000665585.1:c.2576G=
ENST00000680887.1:c.9698G=	ENSP00000505508.1:p.Cys3233=
ENST00000380152.7:c.9698G=	ENSP00000369497.3:p.Cys3233=
ENST00000470094.1:c.781G=
ENST00000533776.1:n.286G=
ENST00000544455.5:c.9698G=	ENSP00000439902.1:p.Cys3233=
NM_000059.3:c.9698G= , LRG_293t1:c.9698G=	NP_000050.2:p.Cys3233=
XM_011535203.1:c.9698G=	XP_011533505.1:p.Cys3233=
XM_011535204.1:c.9602G=	XP_011533506.1:p.Cys3201=
NM_000059.4:c.9698G= MANE Select	NP_000050.3:p.Cys3233=