Canonical Allele Identifier: CA2082835960

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379413G= , CM000675.2:g.32379413G=	GRCh38
NC_000013.10:g.32953550G= , CM000675.1:g.32953550G=	GRCh37
NC_000013.9:g.31851550G=	NCBI36
NG_012772.3:g.68934G= , LRG_293:g.68934G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8851G=	ENSP00000434898.2:p.Ala2951=
ENST00000528762.2:c.*218G=	ENSP00000433168.2:n.*218G=
ENST00000530893.7:c.8482G=	ENSP00000499438.2:p.Ala2828=
ENST00000665585.2:c.*413G=	ENSP00000499570.2:n.*413G=
ENST00000666593.2:c.8851G=	ENSP00000499256.2:p.Ala2951=
ENST00000700202.2:c.8851G=	ENSP00000514856.2:p.Ala2951=
ENST00000700202.1:c.1318G=	ENSP00000514856.1:p.Ala440=
ENST00000700203.1:n.978G=
ENST00000380152.8:c.8851G= MANE Select	ENSP00000369497.3:p.Ala2951=
ENST00000544455.6:c.8851G=	ENSP00000439902.1:p.Ala2951=
ENST00000614259.2:c.8859G=	ENSP00000506251.1:n.8859G=
ENST00000665585.1:c.1729G=
ENST00000680887.1:c.8851G=	ENSP00000505508.1:p.Ala2951=
ENST00000380152.7:c.8851G=	ENSP00000369497.3:p.Ala2951=
ENST00000528762.1:c.413G=	ENSP00000433168.1:n.413G=
ENST00000544455.5:c.8851G=	ENSP00000439902.1:p.Ala2951=
NM_000059.3:c.8851G= , LRG_293t1:c.8851G=	NP_000050.2:p.Ala2951=
XM_011535203.1:c.8851G=	XP_011533505.1:p.Ala2951=
XM_011535204.1:c.8755G=	XP_011533506.1:p.Ala2919=
XM_011535205.1:c.8755-337G=	XP_011533507.1:n.8755-337G=
NM_000059.4:c.8851G= MANE Select	NP_000050.3:p.Ala2951=