Canonical Allele Identifier: CA2082835695
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379369_32379370delinsTG , CM000675.2:g.32379369_32379370delinsTG GRCh38
NC_000013.10:g.32953506_32953507delinsTG , CM000675.1:g.32953506_32953507delinsTG GRCh37
NC_000013.9:g.31851506_31851507delinsTG NCBI36
NG_012772.3:g.68890_68891delinsTG , LRG_293:g.68890_68891delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8807_8808delinsTG ENSP00000434898.2:p.Leu2936=
ENST00000528762.2:c.*174_*175delinsTG ENSP00000433168.2:n.*174_*175delinsTG
ENST00000530893.7:c.8438_8439delinsTG ENSP00000499438.2:p.Leu2813=
ENST00000665585.2:c.*369_*370delinsTG ENSP00000499570.2:n.*369_*370delinsTG
ENST00000666593.2:c.8807_8808delinsTG ENSP00000499256.2:p.Leu2936=
ENST00000700202.2:c.8807_8808delinsTG ENSP00000514856.2:p.Leu2936=
ENST00000700202.1:c.1274_1275delinsTG ENSP00000514856.1:p.Leu425=
ENST00000700203.1:n.934_935delinsTG
ENST00000380152.8:c.8807_8808delinsTG MANE Select ENSP00000369497.3:p.Leu2936=
ENST00000544455.6:c.8807_8808delinsTG ENSP00000439902.1:p.Leu2936=
ENST00000614259.2:c.8815_8816delinsTG ENSP00000506251.1:n.8815_8816delinsTG
ENST00000665585.1:c.1685_1686delinsTG
ENST00000680887.1:c.8807_8808delinsTG ENSP00000505508.1:p.Leu2936=
ENST00000380152.7:c.8807_8808delinsTG ENSP00000369497.3:p.Leu2936=
ENST00000528762.1:c.369_370delinsTG ENSP00000433168.1:n.369_370delinsTG
ENST00000544455.5:c.8807_8808delinsTG ENSP00000439902.1:p.Leu2936=
NM_000059.3:c.8807_8808delinsTG , LRG_293t1:c.8807_8808delinsTG NP_000050.2:p.Leu2936=
XM_011535203.1:c.8807_8808delinsTG XP_011533505.1:p.Leu2936=
XM_011535204.1:c.8711_8712delinsTG XP_011533506.1:p.Leu2904=
XM_011535205.1:c.8755-381_8755-380delinsTG XP_011533507.1:n.8755-381_8755-380delinsTG
NM_000059.4:c.8807_8808delinsTG MANE Select NP_000050.3:p.Leu2936=