Canonical Allele Identifier: CA2580614667
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1425390
ClinVar RCV Id: RCV001926602
dbSNP Id: rs2137501220

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32338272_32338274del , CM000675.2:g.32338272_32338274del GRCh38
NC_000013.10:g.32912409_32912411del , CM000675.1:g.32912409_32912411del GRCh37
NC_000013.9:g.31810409_31810411del NCBI36
NG_012772.3:g.27793_27795del , LRG_293:g.27793_27795del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.3917_3919del ENSP00000434898.2:p.Val1306del
ENST00000528762.2:c.3917_3919del ENSP00000433168.2:p.Val1306del
ENST00000530893.7:c.3548_3550del ENSP00000499438.2:p.Val1183del
ENST00000665585.2:c.3917_3919del ENSP00000499570.2:p.Val1306del
ENST00000666593.2:c.3917_3919del ENSP00000499256.2:p.Val1306del
ENST00000700202.2:c.3917_3919del ENSP00000514856.2:p.Val1306del
ENST00000380152.8:c.3917_3919del MANE Select ENSP00000369497.3:p.Val1306del
ENST00000544455.6:c.3917_3919del ENSP00000439902.1:p.Val1306del
ENST00000614259.2:c.3917_3919del ENSP00000506251.1:p.Val1306del
ENST00000680887.1:c.3917_3919del ENSP00000505508.1:p.Val1306del
ENST00000380152.7:c.3917_3919del ENSP00000369497.3:p.Val1306del
ENST00000544455.5:c.3917_3919del ENSP00000439902.1:p.Val1306del
ENST00000614259.1:n.3917_3919del
NM_000059.3:c.3917_3919del , LRG_293t1:c.3917_3919del NP_000050.2:p.Val1306del
XM_011535203.1:c.3917_3919del XP_011533505.1:p.Val1306del
XM_011535204.1:c.3917_3919del XP_011533506.1:p.Val1306del
XM_011535205.1:c.3917_3919del XP_011533507.1:p.Val1306del
NM_000059.4:c.3917_3919del MANE Select NP_000050.3:p.Val1306del