Canonical Allele Identifier: CA2082828874

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376733A= , CM000675.2:g.32376733A=	GRCh38
NC_000013.10:g.32950870A= , CM000675.1:g.32950870A=	GRCh37
NC_000013.9:g.31848870A=	NCBI36
NG_012772.3:g.66254A= , LRG_293:g.66254A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8696A=	ENSP00000434898.2:p.Gln2899=
ENST00000528762.2:c.*63A=	ENSP00000433168.2:n.*63A=
ENST00000530893.7:c.8327A=	ENSP00000499438.2:p.Gln2776=
ENST00000665585.2:c.*258A=	ENSP00000499570.2:n.*258A=
ENST00000666593.2:c.8696A=	ENSP00000499256.2:p.Gln2899=
ENST00000700202.2:c.8696A=	ENSP00000514856.2:p.Gln2899=
ENST00000700202.1:c.1163A=	ENSP00000514856.1:p.Gln388=
ENST00000700203.1:n.823A=
ENST00000380152.8:c.8696A= MANE Select	ENSP00000369497.3:p.Gln2899=
ENST00000544455.6:c.8696A=	ENSP00000439902.1:p.Gln2899=
ENST00000614259.2:c.8704A=	ENSP00000506251.1:n.8704A=
ENST00000665585.1:c.1574A=
ENST00000680887.1:c.8696A=	ENSP00000505508.1:p.Gln2899=
ENST00000380152.7:c.8696A=	ENSP00000369497.3:p.Gln2899=
ENST00000528762.1:c.258A=	ENSP00000433168.1:n.258A=
ENST00000544455.5:c.8696A=	ENSP00000439902.1:p.Gln2899=
NM_000059.3:c.8696A= , LRG_293t1:c.8696A=	NP_000050.2:p.Gln2899=
XM_011535203.1:c.8696A=	XP_011533505.1:p.Gln2899=
XM_011535204.1:c.8600A=	XP_011533506.1:p.Gln2867=
XM_011535205.1:c.8696A=	XP_011533507.1:p.Gln2899=
NM_000059.4:c.8696A= MANE Select	NP_000050.3:p.Gln2899=