Canonical Allele Identifier: CA2082759598

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32331003_32331008delinsACAAAT , CM000675.2:g.32331003_32331008delinsACAAAT	GRCh38
NC_000013.10:g.32905140_32905145delinsACAAAT , CM000675.1:g.32905140_32905145delinsACAAAT	GRCh37
NC_000013.9:g.31803140_31803145delinsACAAAT	NCBI36
NG_012772.3:g.20524_20529delinsACAAAT , LRG_293:g.20524_20529delinsACAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.766_771delinsACAAAT	ENSP00000434898.2:p.Thr256=
ENST00000528762.2:c.766_771delinsACAAAT	ENSP00000433168.2:p.Thr256=
ENST00000530893.7:c.397_402delinsACAAAT	ENSP00000499438.2:p.Thr133=
ENST00000665585.2:c.766_771delinsACAAAT	ENSP00000499570.2:p.Thr256=
ENST00000666593.2:c.766_771delinsACAAAT	ENSP00000499256.2:p.Thr256=
ENST00000700202.2:c.766_771delinsACAAAT	ENSP00000514856.2:p.Thr256=
ENST00000700201.1:c.*545_*550delinsACAAAT	ENSP00000514855.1:n.*545_*550delinsACAAAT
ENST00000380152.8:c.766_771delinsACAAAT MANE Select	ENSP00000369497.3:p.Thr256=
ENST00000544455.6:c.766_771delinsACAAAT	ENSP00000439902.1:p.Thr256=
ENST00000614259.2:c.766_771delinsACAAAT	ENSP00000506251.1:p.Thr256=
ENST00000680887.1:c.766_771delinsACAAAT	ENSP00000505508.1:p.Thr256=
ENST00000380152.7:c.766_771delinsACAAAT	ENSP00000369497.3:p.Thr256=
ENST00000530893.6:n.964_969delinsACAAAT
ENST00000544455.5:c.766_771delinsACAAAT	ENSP00000439902.1:p.Thr256=
ENST00000614259.1:n.766_771delinsACAAAT
NM_000059.3:c.766_771delinsACAAAT , LRG_293t1:c.766_771delinsACAAAT	NP_000050.2:p.Thr256=
XM_011535203.1:c.766_771delinsACAAAT	XP_011533505.1:p.Thr256=
XM_011535204.1:c.766_771delinsACAAAT	XP_011533506.1:p.Thr256=
XM_011535205.1:c.766_771delinsACAAAT	XP_011533507.1:p.Thr256=
NM_000059.4:c.766_771delinsACAAAT MANE Select	NP_000050.3:p.Thr256=