Canonical Allele Identifier: CA2082818658

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32357866_32357867delinsTG , CM000675.2:g.32357866_32357867delinsTG	GRCh38
NC_000013.10:g.32932003_32932004delinsTG , CM000675.1:g.32932003_32932004delinsTG	GRCh37
NC_000013.9:g.31830003_31830004delinsTG	NCBI36
NG_012772.3:g.47387_47388delinsTG , LRG_293:g.47387_47388delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.7742_7743delinsTG	ENSP00000434898.2:p.Leu2581=
ENST00000528762.2:c.7742_7743delinsTG	ENSP00000433168.2:p.Leu2581=
ENST00000530893.7:c.7373_7374delinsTG	ENSP00000499438.2:p.Leu2458=
ENST00000665585.2:c.7742_7743delinsTG	ENSP00000499570.2:p.Leu2581=
ENST00000666593.2:c.7742_7743delinsTG	ENSP00000499256.2:p.Leu2581=
ENST00000700202.2:c.7742_7743delinsTG	ENSP00000514856.2:p.Leu2581=
ENST00000700202.1:c.209_210delinsTG	ENSP00000514856.1:p.Leu70=
ENST00000380152.8:c.7742_7743delinsTG MANE Select	ENSP00000369497.3:p.Leu2581=
ENST00000544455.6:c.7742_7743delinsTG	ENSP00000439902.1:p.Leu2581=
ENST00000614259.2:c.7742_7743delinsTG	ENSP00000506251.1:p.Leu2581=
ENST00000665585.1:c.307_308delinsTG
ENST00000680887.1:c.7742_7743delinsTG	ENSP00000505508.1:p.Leu2581=
ENST00000380152.7:c.7742_7743delinsTG	ENSP00000369497.3:p.Leu2581=
ENST00000544455.5:c.7742_7743delinsTG	ENSP00000439902.1:p.Leu2581=
ENST00000614259.1:n.7742_7743delinsTG
NM_000059.3:c.7742_7743delinsTG , LRG_293t1:c.7742_7743delinsTG	NP_000050.2:p.Leu2581=
XM_011535203.1:c.7742_7743delinsTG	XP_011533505.1:p.Leu2581=
XM_011535204.1:c.7646_7647delinsTG	XP_011533506.1:p.Leu2549=
XM_011535205.1:c.7742_7743delinsTG	XP_011533507.1:p.Leu2581=
NM_000059.4:c.7742_7743delinsTG MANE Select	NP_000050.3:p.Leu2581=