Canonical Allele Identifier: CA011479
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 37736
dbSNP Id: rs80359276

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32332774_32332775del , CM000675.2:g.32332774_32332775del GRCh38
NC_000013.10:g.32906911_32906912del , CM000675.1:g.32906911_32906912del GRCh37
NC_000013.9:g.31804911_31804912del NCBI36
NG_012772.3:g.22295_22296del , LRG_293:g.22295_22296del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.1296_1297del ENSP00000434898.2:p.Asn433GlnfsTer18
ENST00000528762.2:c.1296_1297del ENSP00000433168.2:p.Asn433GlnfsTer18
ENST00000530893.7:c.927_928del ENSP00000499438.2:p.Asn310GlnfsTer18
ENST00000665585.2:c.1296_1297del ENSP00000499570.2:p.Asn433GlnfsTer18
ENST00000666593.2:c.1296_1297del ENSP00000499256.2:p.Asn433GlnfsTer18
ENST00000700202.2:c.1296_1297del ENSP00000514856.2:p.Asn433GlnfsTer18
ENST00000700201.1:c.*1075_*1076del ENSP00000514855.1:n.*1075_*1076del
ENST00000380152.8:c.1296_1297del MANE Select ENSP00000369497.3:p.Asn433GlnfsTer18
ENST00000544455.6:c.1296_1297del ENSP00000439902.1:p.Asn433GlnfsTer18
ENST00000614259.2:c.1296_1297del ENSP00000506251.1:p.Asn433GlnfsTer18
ENST00000680887.1:c.1296_1297del ENSP00000505508.1:p.Asn433GlnfsTer18
ENST00000380152.7:c.1296_1297del ENSP00000369497.3:p.Asn433GlnfsTer18
ENST00000530893.6:n.1494_1495del
ENST00000544455.5:c.1296_1297del ENSP00000439902.1:p.Asn433GlnfsTer18
ENST00000614259.1:n.1296_1297del
NM_000059.3:c.1296_1297del , LRG_293t1:c.1296_1297del NP_000050.2:p.Asn433GlnfsTer18
XM_011535203.1:c.1296_1297del XP_011533505.1:p.Asn433GlnfsTer18
XM_011535204.1:c.1296_1297del XP_011533506.1:p.Asn433GlnfsTer18
XM_011535205.1:c.1296_1297del XP_011533507.1:p.Asn433GlnfsTer18
NM_000059.4:c.1296_1297del MANE Select NP_000050.3:p.Asn433GlnfsTer18