Canonical Allele Identifier: CA025683
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38166
dbSNP Id: rs80359712

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32370969del , CM000675.2:g.32370969del GRCh38
NC_000013.10:g.32945106del , CM000675.1:g.32945106del GRCh37
NC_000013.9:g.31843106del NCBI36
NG_012772.3:g.60490del , LRG_293:g.60490del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8501del ENSP00000434898.2:p.Thr2834AsnfsTer29
ENST00000528762.2:c.8501del ENSP00000433168.2:p.Thr2834AsnfsTer29
ENST00000530893.7:c.8132del ENSP00000499438.2:p.Thr2711AsnfsTer29
ENST00000665585.2:c.8501del ENSP00000499570.2:p.Thr2834AsnfsTer29
ENST00000666593.2:c.8501del ENSP00000499256.2:p.Thr2834AsnfsTer29
ENST00000700202.2:c.8501del ENSP00000514856.2:p.Thr2834AsnfsTer29
ENST00000700202.1:c.968del ENSP00000514856.1:p.Thr323AsnfsTer29
ENST00000380152.8:c.8501del MANE Select ENSP00000369497.3:p.Thr2834AsnfsTer29
ENST00000544455.6:c.8501del ENSP00000439902.1:p.Thr2834AsnfsTer29
ENST00000614259.2:c.8509del ENSP00000506251.1:n.8509del
ENST00000665585.1:c.1066del
ENST00000680887.1:c.8501del ENSP00000505508.1:p.Thr2834AsnfsTer29
ENST00000380152.7:c.8501del ENSP00000369497.3:p.Thr2834AsnfsTer29
ENST00000544455.5:c.8501del ENSP00000439902.1:p.Thr2834AsnfsTer29
NM_000059.3:c.8501del , LRG_293t1:c.8501del NP_000050.2:p.Thr2834AsnfsTer29
XM_011535203.1:c.8501del XP_011533505.1:p.Thr2834AsnfsTer29
XM_011535204.1:c.8405del XP_011533506.1:p.Thr2802AsnfsTer29
XM_011535205.1:c.8501del XP_011533507.1:p.Thr2834AsnfsTer29
NM_000059.4:c.8501del MANE Select NP_000050.3:p.Thr2834AsnfsTer29