Canonical Allele Identifier: CA2082816948

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339256T= , CM000675.2:g.32339256T=	GRCh38
NC_000013.10:g.32913393T= , CM000675.1:g.32913393T=	GRCh37
NC_000013.9:g.31811393T=	NCBI36
NG_012772.3:g.28777T= , LRG_293:g.28777T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.4901T=	ENSP00000434898.2:p.Phe1634=
ENST00000528762.2:c.4901T=	ENSP00000433168.2:p.Phe1634=
ENST00000530893.7:c.4532T=	ENSP00000499438.2:p.Phe1511=
ENST00000665585.2:c.4901T=	ENSP00000499570.2:p.Phe1634=
ENST00000666593.2:c.4901T=	ENSP00000499256.2:p.Phe1634=
ENST00000700202.2:c.4901T=	ENSP00000514856.2:p.Phe1634=
ENST00000380152.8:c.4901T= MANE Select	ENSP00000369497.3:p.Phe1634=
ENST00000544455.6:c.4901T=	ENSP00000439902.1:p.Phe1634=
ENST00000614259.2:c.4901T=	ENSP00000506251.1:p.Phe1634=
ENST00000680887.1:c.4901T=	ENSP00000505508.1:p.Phe1634=
ENST00000380152.7:c.4901T=	ENSP00000369497.3:p.Phe1634=
ENST00000544455.5:c.4901T=	ENSP00000439902.1:p.Phe1634=
ENST00000614259.1:n.4901T=
NM_000059.3:c.4901T= , LRG_293t1:c.4901T=	NP_000050.2:p.Phe1634=
XM_011535203.1:c.4901T=	XP_011533505.1:p.Phe1634=
XM_011535204.1:c.4901T=	XP_011533506.1:p.Phe1634=
XM_011535205.1:c.4901T=	XP_011533507.1:p.Phe1634=
NM_000059.4:c.4901T= MANE Select	NP_000050.3:p.Phe1634=