Canonical Allele Identifier: CA2082836202

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398466A= , CM000675.2:g.32398466A=	GRCh38
NC_000013.10:g.32972603A= , CM000675.1:g.32972603A=	GRCh37
NC_000013.9:g.31870603A=	NCBI36
NG_012772.3:g.87987A= , LRG_293:g.87987A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*476A=	ENSP00000434898.2:n.*476A=
ENST00000528762.2:c.*1320A=	ENSP00000433168.2:n.*1320A=
ENST00000530893.7:c.9584A=	ENSP00000499438.2:p.Asn3195=
ENST00000665585.2:c.*1515A=	ENSP00000499570.2:n.*1515A=
ENST00000700202.2:c.9902A=	ENSP00000514856.2:p.Asn3301=
ENST00000700202.1:c.2369A=	ENSP00000514856.1:p.Asn790=
ENST00000700203.1:n.2080A=
ENST00000380152.8:c.9953A= MANE Select	ENSP00000369497.3:p.Asn3318=
ENST00000544455.6:c.9953A=	ENSP00000439902.1:p.Asn3318=
ENST00000614259.2:c.9961A=	ENSP00000506251.1:n.9961A=
ENST00000680887.1:c.9953A=	ENSP00000505508.1:p.Asn3318=
ENST00000380152.7:c.9953A=	ENSP00000369497.3:p.Asn3318=
ENST00000544455.5:c.9953A=	ENSP00000439902.1:p.Asn3318=
NM_000059.3:c.9953A= , LRG_293t1:c.9953A=	NP_000050.2:p.Asn3318=
XM_011535203.1:c.9953A=	XP_011533505.1:p.Asn3318=
XM_011535204.1:c.9857A=	XP_011533506.1:p.Asn3286=
NM_000059.4:c.9953A= MANE Select	NP_000050.3:p.Asn3318=