Canonical Allele Identifier: CA2082836565

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379491T= , CM000675.2:g.32379491T=	GRCh38
NC_000013.10:g.32953628T= , CM000675.1:g.32953628T=	GRCh37
NC_000013.9:g.31851628T=	NCBI36
NG_012772.3:g.69012T= , LRG_293:g.69012T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8929T=	ENSP00000434898.2:p.Tyr2977=
ENST00000528762.2:c.*296T=	ENSP00000433168.2:n.*296T=
ENST00000530893.7:c.8560T=	ENSP00000499438.2:p.Tyr2854=
ENST00000665585.2:c.*491T=	ENSP00000499570.2:n.*491T=
ENST00000666593.2:c.8929T=	ENSP00000499256.2:p.Tyr2977=
ENST00000700202.2:c.8929T=	ENSP00000514856.2:p.Tyr2977=
ENST00000700202.1:c.1396T=	ENSP00000514856.1:p.Tyr466=
ENST00000700203.1:n.1056T=
ENST00000380152.8:c.8929T= MANE Select	ENSP00000369497.3:p.Tyr2977=
ENST00000544455.6:c.8929T=	ENSP00000439902.1:p.Tyr2977=
ENST00000614259.2:c.8937T=	ENSP00000506251.1:n.8937T=
ENST00000665585.1:c.1807T=
ENST00000680887.1:c.8929T=	ENSP00000505508.1:p.Tyr2977=
ENST00000380152.7:c.8929T=	ENSP00000369497.3:p.Tyr2977=
ENST00000528762.1:c.491T=	ENSP00000433168.1:n.491T=
ENST00000544455.5:c.8929T=	ENSP00000439902.1:p.Tyr2977=
NM_000059.3:c.8929T= , LRG_293t1:c.8929T=	NP_000050.2:p.Tyr2977=
XM_011535203.1:c.8929T=	XP_011533505.1:p.Tyr2977=
XM_011535204.1:c.8833T=	XP_011533506.1:p.Tyr2945=
XM_011535205.1:c.8755-259T=	XP_011533507.1:n.8755-259T=
NM_000059.4:c.8929T= MANE Select	NP_000050.3:p.Tyr2977=