Canonical Allele Identifier: CA2082814392

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370547A= , CM000675.2:g.32370547A=	GRCh38
NC_000013.10:g.32944684A= , CM000675.1:g.32944684A=	GRCh37
NC_000013.9:g.31842684A=	NCBI36
NG_012772.3:g.60068A= , LRG_293:g.60068A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8477A=	ENSP00000434898.2:p.Tyr2826=
ENST00000528762.2:c.8477A=	ENSP00000433168.2:p.Tyr2826=
ENST00000530893.7:c.8108A=	ENSP00000499438.2:p.Tyr2703=
ENST00000665585.2:c.8477A=	ENSP00000499570.2:p.Tyr2826=
ENST00000666593.2:c.8477A=	ENSP00000499256.2:p.Tyr2826=
ENST00000700202.2:c.8477A=	ENSP00000514856.2:p.Tyr2826=
ENST00000700202.1:c.944A=	ENSP00000514856.1:p.Tyr315=
ENST00000380152.8:c.8477A= MANE Select	ENSP00000369497.3:p.Tyr2826=
ENST00000544455.6:c.8477A=	ENSP00000439902.1:p.Tyr2826=
ENST00000614259.2:c.8485A=	ENSP00000506251.1:n.8485A=
ENST00000665585.1:c.1042A=
ENST00000680887.1:c.8477A=	ENSP00000505508.1:p.Tyr2826=
ENST00000380152.7:c.8477A=	ENSP00000369497.3:p.Tyr2826=
ENST00000544455.5:c.8477A=	ENSP00000439902.1:p.Tyr2826=
NM_000059.3:c.8477A= , LRG_293t1:c.8477A=	NP_000050.2:p.Tyr2826=
XM_011535203.1:c.8477A=	XP_011533505.1:p.Tyr2826=
XM_011535204.1:c.8381A=	XP_011533506.1:p.Tyr2794=
XM_011535205.1:c.8477A=	XP_011533507.1:p.Tyr2826=
NM_000059.4:c.8477A= MANE Select	NP_000050.3:p.Tyr2826=