Canonical Allele Identifier: CA2695218006
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32332732dup , CM000675.2:g.32332732dup GRCh38
NC_000013.10:g.32906869dup , CM000675.1:g.32906869dup GRCh37
NC_000013.9:g.31804869dup NCBI36
NG_012772.3:g.22253dup , LRG_293:g.22253dup

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.1254dup ENSP00000434898.2:p.Cys419MetfsTer2
ENST00000528762.2:c.1254dup ENSP00000433168.2:p.Cys419MetfsTer2
ENST00000530893.7:c.885dup ENSP00000499438.2:p.Cys296MetfsTer2
ENST00000665585.2:c.1254dup ENSP00000499570.2:p.Cys419MetfsTer2
ENST00000666593.2:c.1254dup ENSP00000499256.2:p.Cys419MetfsTer2
ENST00000700202.2:c.1254dup ENSP00000514856.2:p.Cys419MetfsTer2
ENST00000700201.1:c.*1033dup ENSP00000514855.1:n.*1033dup
ENST00000380152.8:c.1254dup MANE Select ENSP00000369497.3:p.Cys419MetfsTer2
ENST00000544455.6:c.1254dup ENSP00000439902.1:p.Cys419MetfsTer2
ENST00000614259.2:c.1254dup ENSP00000506251.1:p.Cys419MetfsTer2
ENST00000680887.1:c.1254dup ENSP00000505508.1:p.Cys419MetfsTer2
ENST00000380152.7:c.1254dup ENSP00000369497.3:p.Cys419MetfsTer2
ENST00000530893.6:n.1452dup
ENST00000544455.5:c.1254dup ENSP00000439902.1:p.Cys419MetfsTer2
ENST00000614259.1:n.1254dup
NM_000059.3:c.1254dup , LRG_293t1:c.1254dup NP_000050.2:p.Cys419MetfsTer2
XM_011535203.1:c.1254dup XP_011533505.1:p.Cys419MetfsTer2
XM_011535204.1:c.1254dup XP_011533506.1:p.Cys419MetfsTer2
XM_011535205.1:c.1254dup XP_011533507.1:p.Cys419MetfsTer2
NM_000059.4:c.1254dup MANE Select NP_000050.3:p.Cys419MetfsTer2