Canonical Allele Identifier: CA2573149376
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372712
ClinVar RCV Id: RCV001874772
dbSNP Id: rs2137485485

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32336694_32336707del , CM000675.2:g.32336694_32336707del GRCh38
NC_000013.10:g.32910831_32910844del , CM000675.1:g.32910831_32910844del GRCh37
NC_000013.9:g.31808831_31808844del NCBI36
NG_012772.3:g.26215_26228del , LRG_293:g.26215_26228del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.2339_2352del ENSP00000434898.2:p.Ser780TyrfsTer3
ENST00000528762.2:c.2339_2352del ENSP00000433168.2:p.Ser780TyrfsTer3
ENST00000530893.7:c.1970_1983del ENSP00000499438.2:p.Ser657TyrfsTer3
ENST00000665585.2:c.2339_2352del ENSP00000499570.2:p.Ser780TyrfsTer3
ENST00000666593.2:c.2339_2352del ENSP00000499256.2:p.Ser780TyrfsTer3
ENST00000700202.2:c.2339_2352del ENSP00000514856.2:p.Ser780TyrfsTer3
ENST00000380152.8:c.2339_2352del MANE Select ENSP00000369497.3:p.Ser780TyrfsTer3
ENST00000544455.6:c.2339_2352del ENSP00000439902.1:p.Ser780TyrfsTer3
ENST00000614259.2:c.2339_2352del ENSP00000506251.1:p.Ser780TyrfsTer3
ENST00000680887.1:c.2339_2352del ENSP00000505508.1:p.Ser780TyrfsTer3
ENST00000380152.7:c.2339_2352del ENSP00000369497.3:p.Ser780TyrfsTer3
ENST00000544455.5:c.2339_2352del ENSP00000439902.1:p.Ser780TyrfsTer3
ENST00000614259.1:n.2339_2352del
NM_000059.3:c.2339_2352del , LRG_293t1:c.2339_2352del NP_000050.2:p.Ser780TyrfsTer3
XM_011535203.1:c.2339_2352del XP_011533505.1:p.Ser780TyrfsTer3
XM_011535204.1:c.2339_2352del XP_011533506.1:p.Ser780TyrfsTer3
XM_011535205.1:c.2339_2352del XP_011533507.1:p.Ser780TyrfsTer3
NM_000059.4:c.2339_2352del MANE Select NP_000050.3:p.Ser780TyrfsTer3