Canonical Allele Identifier: CA2082840795

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32380096T= , CM000675.2:g.32380096T=	GRCh38
NC_000013.10:g.32954233T= , CM000675.1:g.32954233T=	GRCh37
NC_000013.9:g.31852233T=	NCBI36
NG_012772.3:g.69617T= , LRG_293:g.69617T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9207T= MANE Select	NP_000050.3:p.Cys3069=
ENST00000380152.8:c.9207T= MANE Select	ENSP00000369497.3:p.Cys3069=
NM_000059.3:c.9207T= , LRG_293t1:c.9207T=	NP_000050.2:p.Cys3069=
ENST00000380152.7:c.9207T=	ENSP00000369497.3:p.Cys3069=
ENST00000470094.1:c.164T=
ENST00000470094.2:c.9207T=	ENSP00000434898.2:p.Cys3069=
ENST00000528762.2:c.*574T=	ENSP00000433168.2:n.*574T=
ENST00000530893.7:c.8838T=	ENSP00000499438.2:p.Cys2946=
ENST00000544455.5:c.9207T=	ENSP00000439902.1:p.Cys3069=
ENST00000544455.6:c.9207T=	ENSP00000439902.1:p.Cys3069=
ENST00000614259.2:c.9215T=	ENSP00000506251.1:n.9215T=
ENST00000665585.1:c.2085T=
ENST00000665585.2:c.*769T=	ENSP00000499570.2:n.*769T=
ENST00000666593.1:c.90T=	ENSP00000499256.1:p.Cys30=
ENST00000666593.2:c.9207T=	ENSP00000499256.2:p.Cys3069=
ENST00000680887.1:c.9207T=	ENSP00000505508.1:p.Cys3069=
ENST00000700202.1:c.1623T=	ENSP00000514856.1:p.Cys541=
ENST00000700202.2:c.9156T=	ENSP00000514856.2:p.Cys3052=
ENST00000700203.1:n.1334T=
XM_011535203.1:c.9207T=	XP_011533505.1:p.Cys3069=
XM_011535204.1:c.9111T=	XP_011533506.1:p.Cys3037=