Canonical Allele Identifier: CA1139655033
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32336302del , CM000675.2:g.32336302del GRCh38
NC_000013.10:g.32910439del , CM000675.1:g.32910439del GRCh37
NC_000013.9:g.31808439del NCBI36
NG_012772.3:g.25823del , LRG_293:g.25823del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.1947del ENSP00000434898.2:p.Asn650MetfsTer10
ENST00000528762.2:c.1947del ENSP00000433168.2:p.Asn650MetfsTer10
ENST00000530893.7:c.1578del ENSP00000499438.2:p.Asn527MetfsTer10
ENST00000665585.2:c.1947del ENSP00000499570.2:p.Asn650MetfsTer10
ENST00000666593.2:c.1947del ENSP00000499256.2:p.Asn650MetfsTer10
ENST00000700202.2:c.1947del ENSP00000514856.2:p.Asn650MetfsTer10
ENST00000380152.8:c.1947del MANE Select ENSP00000369497.3:p.Asn650MetfsTer10
ENST00000544455.6:c.1947del ENSP00000439902.1:p.Asn650MetfsTer10
ENST00000614259.2:c.1947del ENSP00000506251.1:p.Asn650MetfsTer10
ENST00000680887.1:c.1947del ENSP00000505508.1:p.Asn650MetfsTer10
ENST00000380152.7:c.1947del ENSP00000369497.3:p.Asn650MetfsTer10
ENST00000544455.5:c.1947del ENSP00000439902.1:p.Asn650MetfsTer10
ENST00000614259.1:n.1947del
NM_000059.3:c.1947del , LRG_293t1:c.1947del NP_000050.2:p.Asn650MetfsTer10
XM_011535203.1:c.1947del XP_011533505.1:p.Asn650MetfsTer10
XM_011535204.1:c.1947del XP_011533506.1:p.Asn650MetfsTer10
XM_011535205.1:c.1947del XP_011533507.1:p.Asn650MetfsTer10
NM_000059.4:c.1947del MANE Select NP_000050.3:p.Asn650MetfsTer10