Canonical Allele Identifier: CA2082782417

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319094_32319096delinsCTT , CM000675.2:g.32319094_32319096delinsCTT	GRCh38
NC_000013.10:g.32893231_32893233delinsCTT , CM000675.1:g.32893231_32893233delinsCTT	GRCh37
NC_000013.9:g.31791231_31791233delinsCTT	NCBI36
NG_012772.3:g.8615_8617delinsCTT , LRG_293:g.8615_8617delinsCTT
NG_017006.2:g.1268_1270delinsAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.85_87delinsCTT	ENSP00000434898.2:p.Leu29=
ENST00000528762.2:c.85_87delinsCTT	ENSP00000433168.2:p.Leu29=
ENST00000530893.7:c.-285_-283delinsCTT	ENSP00000499438.2:n.-285_-283delinsCTT
ENST00000665585.2:c.85_87delinsCTT	ENSP00000499570.2:p.Leu29=
ENST00000666593.2:c.85_87delinsCTT	ENSP00000499256.2:p.Leu29=
ENST00000700202.2:c.85_87delinsCTT	ENSP00000514856.2:p.Leu29=
ENST00000700200.1:n.191+2567_191+2569delinsCTT
ENST00000700201.1:c.85_87delinsCTT	ENSP00000514855.1:p.Leu29=
ENST00000380152.8:c.85_87delinsCTT MANE Select	ENSP00000369497.3:p.Leu29=
ENST00000544455.6:c.85_87delinsCTT	ENSP00000439902.1:p.Leu29=
ENST00000614259.2:c.85_87delinsCTT	ENSP00000506251.1:p.Leu29=
ENST00000680887.1:c.85_87delinsCTT	ENSP00000505508.1:p.Leu29=
ENST00000380152.7:c.85_87delinsCTT	ENSP00000369497.3:p.Leu29=
ENST00000530893.6:n.283_285delinsCTT
ENST00000544455.5:c.85_87delinsCTT	ENSP00000439902.1:p.Leu29=
ENST00000614259.1:n.85_87delinsCTT
NM_000059.3:c.85_87delinsCTT , LRG_293t1:c.85_87delinsCTT	NP_000050.2:p.Leu29=
XM_011535203.1:c.85_87delinsCTT	XP_011533505.1:p.Leu29=
XM_011535204.1:c.85_87delinsCTT	XP_011533506.1:p.Leu29=
XM_011535205.1:c.85_87delinsCTT	XP_011533507.1:p.Leu29=
NM_000059.4:c.85_87delinsCTT MANE Select	NP_000050.3:p.Leu29=