Canonical Allele Identifier: CA2082835240

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398313A= , CM000675.2:g.32398313A=	GRCh38
NC_000013.10:g.32972450A= , CM000675.1:g.32972450A=	GRCh37
NC_000013.9:g.31870450A=	NCBI36
NG_012772.3:g.87834A= , LRG_293:g.87834A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*323A=	ENSP00000434898.2:n.*323A=
ENST00000528762.2:c.*1167A=	ENSP00000433168.2:n.*1167A=
ENST00000530893.7:c.9431A=	ENSP00000499438.2:p.Lys3144=
ENST00000665585.2:c.*1362A=	ENSP00000499570.2:n.*1362A=
ENST00000700202.2:c.9749A=	ENSP00000514856.2:p.Lys3250=
ENST00000700202.1:c.2216A=	ENSP00000514856.1:p.Lys739=
ENST00000700203.1:n.1927A=
ENST00000380152.8:c.9800A= MANE Select	ENSP00000369497.3:p.Lys3267=
ENST00000544455.6:c.9800A=	ENSP00000439902.1:p.Lys3267=
ENST00000614259.2:c.9808A=	ENSP00000506251.1:n.9808A=
ENST00000680887.1:c.9800A=	ENSP00000505508.1:p.Lys3267=
ENST00000380152.7:c.9800A=	ENSP00000369497.3:p.Lys3267=
ENST00000533776.1:n.388A=
ENST00000544455.5:c.9800A=	ENSP00000439902.1:p.Lys3267=
NM_000059.3:c.9800A= , LRG_293t1:c.9800A=	NP_000050.2:p.Lys3267=
XM_011535203.1:c.9800A=	XP_011533505.1:p.Lys3267=
XM_011535204.1:c.9704A=	XP_011533506.1:p.Lys3235=
NM_000059.4:c.9800A= MANE Select	NP_000050.3:p.Lys3267=