Canonical Allele Identifier: CA891842148
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32332916_32332929del , CM000675.2:g.32332916_32332929del GRCh38
NC_000013.10:g.32907053_32907066del , CM000675.1:g.32907053_32907066del GRCh37
NC_000013.9:g.31805053_31805066del NCBI36
NG_012772.3:g.22437_22450del , LRG_293:g.22437_22450del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.1438_1451del ENSP00000434898.2:p.Cys480LysfsTer29
ENST00000528762.2:c.1438_1451del ENSP00000433168.2:p.Cys480LysfsTer29
ENST00000530893.7:c.1069_1082del ENSP00000499438.2:p.Cys357LysfsTer29
ENST00000665585.2:c.1438_1451del ENSP00000499570.2:p.Cys480LysfsTer29
ENST00000666593.2:c.1438_1451del ENSP00000499256.2:p.Cys480LysfsTer29
ENST00000700202.2:c.1438_1451del ENSP00000514856.2:p.Cys480LysfsTer29
ENST00000700201.1:c.*1217_*1230del ENSP00000514855.1:n.*1217_*1230del
ENST00000380152.8:c.1438_1451del MANE Select ENSP00000369497.3:p.Cys480LysfsTer29
ENST00000544455.6:c.1438_1451del ENSP00000439902.1:p.Cys480LysfsTer29
ENST00000614259.2:c.1438_1451del ENSP00000506251.1:p.Cys480LysfsTer29
ENST00000680887.1:c.1438_1451del ENSP00000505508.1:p.Cys480LysfsTer29
ENST00000380152.7:c.1438_1451del ENSP00000369497.3:p.Cys480LysfsTer29
ENST00000530893.6:n.1636_1649del
ENST00000544455.5:c.1438_1451del ENSP00000439902.1:p.Cys480LysfsTer29
ENST00000614259.1:n.1438_1451del
NM_000059.3:c.1438_1451del , LRG_293t1:c.1438_1451del NP_000050.2:p.Cys480LysfsTer29
XM_011535203.1:c.1438_1451del XP_011533505.1:p.Cys480LysfsTer29
XM_011535204.1:c.1438_1451del XP_011533506.1:p.Cys480LysfsTer29
XM_011535205.1:c.1438_1451del XP_011533507.1:p.Cys480LysfsTer29
NM_000059.4:c.1438_1451del MANE Select NP_000050.3:p.Cys480LysfsTer29