Canonical Allele Identifier: CA2082831012

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362593_32362594delinsTG , CM000675.2:g.32362593_32362594delinsTG	GRCh38
NC_000013.10:g.32936730_32936731delinsTG , CM000675.1:g.32936730_32936731delinsTG	GRCh37
NC_000013.9:g.31834730_31834731delinsTG	NCBI36
NG_012772.3:g.52114_52115delinsTG , LRG_293:g.52114_52115delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.7876_7877delinsTG	ENSP00000434898.2:p.Trp2626=
ENST00000528762.2:c.7876_7877delinsTG	ENSP00000433168.2:p.Trp2626=
ENST00000530893.7:c.7507_7508delinsTG	ENSP00000499438.2:p.Trp2503=
ENST00000665585.2:c.7876_7877delinsTG	ENSP00000499570.2:p.Trp2626=
ENST00000666593.2:c.7876_7877delinsTG	ENSP00000499256.2:p.Trp2626=
ENST00000700202.2:c.7876_7877delinsTG	ENSP00000514856.2:p.Trp2626=
ENST00000700202.1:c.343_344delinsTG	ENSP00000514856.1:p.Trp115=
ENST00000380152.8:c.7876_7877delinsTG MANE Select	ENSP00000369497.3:p.Trp2626=
ENST00000544455.6:c.7876_7877delinsTG	ENSP00000439902.1:p.Trp2626=
ENST00000614259.2:c.7884_7885delinsTG	ENSP00000506251.1:p.Asp2628=
ENST00000665585.1:c.441_442delinsTG
ENST00000680887.1:c.7876_7877delinsTG	ENSP00000505508.1:p.Trp2626=
ENST00000380152.7:c.7876_7877delinsTG	ENSP00000369497.3:p.Trp2626=
ENST00000544455.5:c.7876_7877delinsTG	ENSP00000439902.1:p.Trp2626=
ENST00000614259.1:n.7884_7885delinsTG
NM_000059.3:c.7876_7877delinsTG , LRG_293t1:c.7876_7877delinsTG	NP_000050.2:p.Trp2626=
XM_011535203.1:c.7876_7877delinsTG	XP_011533505.1:p.Trp2626=
XM_011535204.1:c.7780_7781delinsTG	XP_011533506.1:p.Trp2594=
XM_011535205.1:c.7876_7877delinsTG	XP_011533507.1:p.Trp2626=
NM_000059.4:c.7876_7877delinsTG MANE Select	NP_000050.3:p.Trp2626=