Canonical Allele Identifier: CA609453994
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1446081436

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32370856del , CM000675.2:g.32370856del GRCh38
NC_000013.10:g.32944993del , CM000675.1:g.32944993del GRCh37
NC_000013.9:g.31842993del NCBI36
NG_012772.3:g.60377del , LRG_293:g.60377del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8488-100del ENSP00000434898.2:n.8488-100del
ENST00000528762.2:c.8488-100del ENSP00000433168.2:n.8488-100del
ENST00000530893.7:c.8119-100del ENSP00000499438.2:n.8119-100del
ENST00000665585.2:c.8488-100del ENSP00000499570.2:n.8488-100del
ENST00000666593.2:c.8488-100del ENSP00000499256.2:n.8488-100del
ENST00000700202.2:c.8488-100del ENSP00000514856.2:n.8488-100del
ENST00000700202.1:c.955-100del ENSP00000514856.1:n.955-100del
ENST00000380152.8:c.8488-100del MANE Select ENSP00000369497.3:n.8488-100del
ENST00000544455.6:c.8488-100del ENSP00000439902.1:n.8488-100del
ENST00000614259.2:c.8496-100del ENSP00000506251.1:n.8496-100del
ENST00000665585.1:c.1053-100del
ENST00000680887.1:c.8488-100del ENSP00000505508.1:n.8488-100del
ENST00000380152.7:c.8488-100del ENSP00000369497.3:n.8488-100del
ENST00000544455.5:c.8488-100del ENSP00000439902.1:n.8488-100del
NM_000059.3:c.8488-100del , LRG_293t1:c.8488-100del NP_000050.2:n.8488-100del
XM_011535203.1:c.8488-100del XP_011533505.1:n.8488-100del
XM_011535204.1:c.8392-100del XP_011533506.1:n.8392-100del
XM_011535205.1:c.8488-100del XP_011533507.1:n.8488-100del
NM_000059.4:c.8488-100del MANE Select NP_000050.3:n.8488-100del