Canonical Allele Identifier: CA020582
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 51687
dbSNP Id: rs397507734

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32339002_32339005del , CM000675.2:g.32339002_32339005del GRCh38
NC_000013.10:g.32913139_32913142del , CM000675.1:g.32913139_32913142del GRCh37
NC_000013.9:g.31811139_31811142del NCBI36
NG_012772.3:g.28523_28526del , LRG_293:g.28523_28526del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.4647_4650del ENSP00000434898.2:p.Lys1549AsnfsTer18
ENST00000528762.2:c.4647_4650del ENSP00000433168.2:p.Lys1549AsnfsTer18
ENST00000530893.7:c.4278_4281del ENSP00000499438.2:p.Lys1426AsnfsTer18
ENST00000665585.2:c.4647_4650del ENSP00000499570.2:p.Lys1549AsnfsTer18
ENST00000666593.2:c.4647_4650del ENSP00000499256.2:p.Lys1549AsnfsTer18
ENST00000700202.2:c.4647_4650del ENSP00000514856.2:p.Lys1549AsnfsTer18
ENST00000380152.8:c.4647_4650del MANE Select ENSP00000369497.3:p.Lys1549AsnfsTer18
ENST00000544455.6:c.4647_4650del ENSP00000439902.1:p.Lys1549AsnfsTer18
ENST00000614259.2:c.4647_4650del ENSP00000506251.1:p.Lys1549AsnfsTer18
ENST00000680887.1:c.4647_4650del ENSP00000505508.1:p.Lys1549AsnfsTer18
ENST00000380152.7:c.4647_4650del ENSP00000369497.3:p.Lys1549AsnfsTer18
ENST00000544455.5:c.4647_4650del ENSP00000439902.1:p.Lys1549AsnfsTer18
ENST00000614259.1:n.4647_4650del
NM_000059.3:c.4647_4650del , LRG_293t1:c.4647_4650del NP_000050.2:p.Lys1549AsnfsTer18
XM_011535203.1:c.4647_4650del XP_011533505.1:p.Lys1549AsnfsTer18
XM_011535204.1:c.4647_4650del XP_011533506.1:p.Lys1549AsnfsTer18
XM_011535205.1:c.4647_4650del XP_011533507.1:p.Lys1549AsnfsTer18
NM_000059.4:c.4647_4650del MANE Select NP_000050.3:p.Lys1549AsnfsTer18