Canonical Allele Identifier: CA2082836860

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398574_32398575delinsCT , CM000675.2:g.32398574_32398575delinsCT	GRCh38
NC_000013.10:g.32972711_32972712delinsCT , CM000675.1:g.32972711_32972712delinsCT	GRCh37
NC_000013.9:g.31870711_31870712delinsCT	NCBI36
NG_012772.3:g.88095_88096delinsCT , LRG_293:g.88095_88096delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*584_*585delinsCT	ENSP00000434898.2:n.*584_*585delinsCT
ENST00000528762.2:c.*1428_*1429delinsCT	ENSP00000433168.2:n.*1428_*1429delinsCT
ENST00000530893.7:c.9692_9693delinsCT	ENSP00000499438.2:p.Ser3231=
ENST00000665585.2:c.*1623_*1624delinsCT	ENSP00000499570.2:n.*1623_*1624delinsCT
ENST00000700202.2:c.10010_10011delinsCT	ENSP00000514856.2:p.Ser3337=
ENST00000700202.1:c.2477_2478delinsCT	ENSP00000514856.1:p.Ser826=
ENST00000700203.1:n.2188_2189delinsCT
ENST00000380152.8:c.10061_10062delinsCT MANE Select	ENSP00000369497.3:p.Ser3354=
ENST00000544455.6:c.10061_10062delinsCT	ENSP00000439902.1:p.Ser3354=
ENST00000614259.2:c.10069_10070delinsCT	ENSP00000506251.1:n.10069_10070delinsCT
ENST00000680887.1:c.10061_10062delinsCT	ENSP00000505508.1:p.Ser3354=
ENST00000380152.7:c.10061_10062delinsCT	ENSP00000369497.3:p.Ser3354=
ENST00000544455.5:c.10061_10062delinsCT	ENSP00000439902.1:p.Ser3354=
NM_000059.3:c.10061_10062delinsCT , LRG_293t1:c.10061_10062delinsCT	NP_000050.2:p.Ser3354=
XM_011535203.1:c.10061_10062delinsCT	XP_011533505.1:p.Ser3354=
XM_011535204.1:c.9965_9966delinsCT	XP_011533506.1:p.Ser3322=
NM_000059.4:c.10061_10062delinsCT MANE Select	NP_000050.3:p.Ser3354=