Canonical Allele Identifier: CA2082828438

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376693C= , CM000675.2:g.32376693C=	GRCh38
NC_000013.10:g.32950830C= , CM000675.1:g.32950830C=	GRCh37
NC_000013.9:g.31848830C=	NCBI36
NG_012772.3:g.66214C= , LRG_293:g.66214C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8656C=	ENSP00000434898.2:p.Pro2886=
ENST00000528762.2:c.*23C=	ENSP00000433168.2:n.*23C=
ENST00000530893.7:c.8287C=	ENSP00000499438.2:p.Pro2763=
ENST00000665585.2:c.*218C=	ENSP00000499570.2:n.*218C=
ENST00000666593.2:c.8656C=	ENSP00000499256.2:p.Pro2886=
ENST00000700202.2:c.8656C=	ENSP00000514856.2:p.Pro2886=
ENST00000700202.1:c.1123C=	ENSP00000514856.1:p.Pro375=
ENST00000700203.1:n.783C=
ENST00000380152.8:c.8656C= MANE Select	ENSP00000369497.3:p.Pro2886=
ENST00000544455.6:c.8656C=	ENSP00000439902.1:p.Pro2886=
ENST00000614259.2:c.8664C=	ENSP00000506251.1:n.8664C=
ENST00000665585.1:c.1534C=
ENST00000680887.1:c.8656C=	ENSP00000505508.1:p.Pro2886=
ENST00000380152.7:c.8656C=	ENSP00000369497.3:p.Pro2886=
ENST00000528762.1:c.218C=	ENSP00000433168.1:n.218C=
ENST00000544455.5:c.8656C=	ENSP00000439902.1:p.Pro2886=
NM_000059.3:c.8656C= , LRG_293t1:c.8656C=	NP_000050.2:p.Pro2886=
XM_011535203.1:c.8656C=	XP_011533505.1:p.Pro2886=
XM_011535204.1:c.8560C=	XP_011533506.1:p.Pro2854=
XM_011535205.1:c.8656C=	XP_011533507.1:p.Pro2886=
NM_000059.4:c.8656C= MANE Select	NP_000050.3:p.Pro2886=