Canonical Allele Identifier: CA2622599890
Gene: BRCA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32340705_32340713del , CM000675.2:g.32340705_32340713del GRCh38
NC_000013.10:g.32914842_32914850del , CM000675.1:g.32914842_32914850del GRCh37
NC_000013.9:g.31812842_31812850del NCBI36
NG_012772.3:g.30226_30234del , LRG_293:g.30226_30234del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.6350_6358del ENSP00000434898.2:p.Cys2117_Asn2119del
ENST00000528762.2:c.6350_6358del ENSP00000433168.2:p.Cys2117_Asn2119del
ENST00000530893.7:c.5981_5989del ENSP00000499438.2:p.Cys1994_Asn1996del
ENST00000665585.2:c.6350_6358del ENSP00000499570.2:p.Cys2117_Asn2119del
ENST00000666593.2:c.6350_6358del ENSP00000499256.2:p.Cys2117_Asn2119del
ENST00000700202.2:c.6350_6358del ENSP00000514856.2:p.Cys2117_Asn2119del
ENST00000380152.8:c.6350_6358del MANE Select ENSP00000369497.3:p.Cys2117_Asn2119del
ENST00000544455.6:c.6350_6358del ENSP00000439902.1:p.Cys2117_Asn2119del
ENST00000614259.2:c.6350_6358del ENSP00000506251.1:p.Cys2117_Asn2119del
ENST00000680887.1:c.6350_6358del ENSP00000505508.1:p.Cys2117_Asn2119del
ENST00000380152.7:c.6350_6358del ENSP00000369497.3:p.Cys2117_Asn2119del
ENST00000544455.5:c.6350_6358del ENSP00000439902.1:p.Cys2117_Asn2119del
ENST00000614259.1:n.6350_6358del
NM_000059.3:c.6350_6358del , LRG_293t1:c.6350_6358del NP_000050.2:p.Cys2117_Asn2119del
XM_011535203.1:c.6350_6358del XP_011533505.1:p.Cys2117_Asn2119del
XM_011535204.1:c.6350_6358del XP_011533506.1:p.Cys2117_Asn2119del
XM_011535205.1:c.6350_6358del XP_011533507.1:p.Cys2117_Asn2119del
NM_000059.4:c.6350_6358del MANE Select NP_000050.3:p.Cys2117_Asn2119del