Canonical Allele Identifier: CA2082751186
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32326294_32326295delinsAC , CM000675.2:g.32326294_32326295delinsAC GRCh38
NC_000013.10:g.32900431_32900432delinsAC , CM000675.1:g.32900431_32900432delinsAC GRCh37
NC_000013.9:g.31798431_31798432delinsAC NCBI36
NG_012772.3:g.15815_15816delinsAC , LRG_293:g.15815_15816delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.516+12_516+13delinsAC ENSP00000434898.2:n.516+12_516+13delinsAC
ENST00000528762.2:c.516+12_516+13delinsAC ENSP00000433168.2:n.516+12_516+13delinsAC
ENST00000530893.7:c.147+12_147+13delinsAC ENSP00000499438.2:n.147+12_147+13delinsAC
ENST00000665585.2:c.516+12_516+13delinsAC ENSP00000499570.2:n.516+12_516+13delinsAC
ENST00000666593.2:c.516+12_516+13delinsAC ENSP00000499256.2:n.516+12_516+13delinsAC
ENST00000700202.2:c.516+12_516+13delinsAC ENSP00000514856.2:n.516+12_516+13delinsAC
ENST00000700200.1:n.387+12_387+13delinsAC
ENST00000700201.1:c.*295+12_*295+13delinsAC ENSP00000514855.1:n.*295+12_*295+13delinsAC
ENST00000380152.8:c.516+12_516+13delinsAC MANE Select ENSP00000369497.3:n.516+12_516+13delinsAC
ENST00000544455.6:c.516+12_516+13delinsAC ENSP00000439902.1:n.516+12_516+13delinsAC
ENST00000614259.2:c.516+12_516+13delinsAC ENSP00000506251.1:n.516+12_516+13delinsAC
ENST00000680887.1:c.516+12_516+13delinsAC ENSP00000505508.1:n.516+12_516+13delinsAC
ENST00000380152.7:c.516+12_516+13delinsAC ENSP00000369497.3:n.516+12_516+13delinsAC
ENST00000530893.6:n.714+12_714+13delinsAC
ENST00000544455.5:c.516+12_516+13delinsAC ENSP00000439902.1:n.516+12_516+13delinsAC
ENST00000614259.1:n.516+12_516+13delinsAC
NM_000059.3:c.516+12_516+13delinsAC , LRG_293t1:c.516+12_516+13delinsAC NP_000050.2:n.516+12_516+13delinsAC
XM_011535203.1:c.516+12_516+13delinsAC XP_011533505.1:n.516+12_516+13delinsAC
XM_011535204.1:c.516+12_516+13delinsAC XP_011533506.1:n.516+12_516+13delinsAC
XM_011535205.1:c.516+12_516+13delinsAC XP_011533507.1:n.516+12_516+13delinsAC
NM_000059.4:c.516+12_516+13delinsAC MANE Select NP_000050.3:n.516+12_516+13delinsAC