Canonical Allele Identifier: CA2082816266

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371057_32371060delinsAGCC , CM000675.2:g.32371057_32371060delinsAGCC	GRCh38
NC_000013.10:g.32945194_32945197delinsAGCC , CM000675.1:g.32945194_32945197delinsAGCC	GRCh37
NC_000013.9:g.31843194_31843197delinsAGCC	NCBI36
NG_012772.3:g.60578_60581delinsAGCC , LRG_293:g.60578_60581delinsAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8589_8592delinsAGCC	ENSP00000434898.2:p.Glu2863=
ENST00000528762.2:c.8589_8592delinsAGCC	ENSP00000433168.2:p.Glu2863=
ENST00000530893.7:c.8220_8223delinsAGCC	ENSP00000499438.2:p.Glu2740=
ENST00000665585.2:c.8589_8592delinsAGCC	ENSP00000499570.2:p.Glu2863=
ENST00000666593.2:c.8589_8592delinsAGCC	ENSP00000499256.2:p.Glu2863=
ENST00000700202.2:c.8589_8592delinsAGCC	ENSP00000514856.2:p.Glu2863=
ENST00000700202.1:c.1056_1059delinsAGCC	ENSP00000514856.1:p.Glu352=
ENST00000380152.8:c.8589_8592delinsAGCC MANE Select	ENSP00000369497.3:p.Glu2863=
ENST00000544455.6:c.8589_8592delinsAGCC	ENSP00000439902.1:p.Glu2863=
ENST00000614259.2:c.8597_8600delinsAGCC	ENSP00000506251.1:n.8597_8600delinsAGCC
ENST00000665585.1:c.1154_1157delinsAGCC
ENST00000680887.1:c.8589_8592delinsAGCC	ENSP00000505508.1:p.Glu2863=
ENST00000380152.7:c.8589_8592delinsAGCC	ENSP00000369497.3:p.Glu2863=
ENST00000528762.1:c.87_90delinsAGCC	ENSP00000433168.1:p.Glu29=
ENST00000544455.5:c.8589_8592delinsAGCC	ENSP00000439902.1:p.Glu2863=
NM_000059.3:c.8589_8592delinsAGCC , LRG_293t1:c.8589_8592delinsAGCC	NP_000050.2:p.Glu2863=
XM_011535203.1:c.8589_8592delinsAGCC	XP_011533505.1:p.Glu2863=
XM_011535204.1:c.8493_8496delinsAGCC	XP_011533506.1:p.Glu2831=
XM_011535205.1:c.8589_8592delinsAGCC	XP_011533507.1:p.Glu2863=
NM_000059.4:c.8589_8592delinsAGCC MANE Select	NP_000050.3:p.Glu2863=