Canonical Allele Identifier: CA019828
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32326089_32326093del , CM000675.2:g.32326089_32326093del GRCh38
NC_000013.10:g.32900226_32900230del , CM000675.1:g.32900226_32900230del GRCh37
NC_000013.9:g.31798226_31798230del NCBI36
NG_012772.3:g.15610_15614del , LRG_293:g.15610_15614del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.426-12_426-8del ENSP00000434898.2:n.426-12_426-8del
ENST00000528762.2:c.426-12_426-8del ENSP00000433168.2:n.426-12_426-8del
ENST00000530893.7:c.57-12_57-8del ENSP00000499438.2:n.57-12_57-8del
ENST00000665585.2:c.426-12_426-8del ENSP00000499570.2:n.426-12_426-8del
ENST00000666593.2:c.426-12_426-8del ENSP00000499256.2:n.426-12_426-8del
ENST00000700202.2:c.426-12_426-8del ENSP00000514856.2:n.426-12_426-8del
ENST00000700200.1:n.297-12_297-8del
ENST00000700201.1:c.*205-12_*205-8del ENSP00000514855.1:n.*205-12_*205-8del
ENST00000380152.8:c.426-12_426-8del MANE Select ENSP00000369497.3:n.426-12_426-8del
ENST00000544455.6:c.426-12_426-8del ENSP00000439902.1:n.426-12_426-8del
ENST00000614259.2:c.426-12_426-8del ENSP00000506251.1:n.426-12_426-8del
ENST00000680887.1:c.426-12_426-8del ENSP00000505508.1:n.426-12_426-8del
ENST00000380152.7:c.426-12_426-8del ENSP00000369497.3:n.426-12_426-8del
ENST00000530893.6:n.624-12_624-8del
ENST00000544455.5:c.426-12_426-8del ENSP00000439902.1:n.426-12_426-8del
ENST00000614259.1:n.426-12_426-8del
NM_000059.3:c.426-12_426-8del , LRG_293t1:c.426-12_426-8del NP_000050.2:n.426-12_426-8del
XM_011535203.1:c.426-12_426-8del XP_011533505.1:n.426-12_426-8del
XM_011535204.1:c.426-12_426-8del XP_011533506.1:n.426-12_426-8del
XM_011535205.1:c.426-12_426-8del XP_011533507.1:n.426-12_426-8del
NM_000059.4:c.426-12_426-8del MANE Select NP_000050.3:n.426-12_426-8del