Canonical Allele Identifier: CA2082750077
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32326135_32326137delinsCAA , CM000675.2:g.32326135_32326137delinsCAA GRCh38
NC_000013.10:g.32900272_32900274delinsCAA , CM000675.1:g.32900272_32900274delinsCAA GRCh37
NC_000013.9:g.31798272_31798274delinsCAA NCBI36
NG_012772.3:g.15656_15658delinsCAA , LRG_293:g.15656_15658delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.460_462delinsCAA ENSP00000434898.2:p.Gln154=
ENST00000528762.2:c.460_462delinsCAA ENSP00000433168.2:p.Gln154=
ENST00000530893.7:c.91_93delinsCAA ENSP00000499438.2:p.Gln31=
ENST00000665585.2:c.460_462delinsCAA ENSP00000499570.2:p.Gln154=
ENST00000666593.2:c.460_462delinsCAA ENSP00000499256.2:p.Gln154=
ENST00000700202.2:c.460_462delinsCAA ENSP00000514856.2:p.Gln154=
ENST00000700200.1:n.331_333delinsCAA
ENST00000700201.1:c.*239_*241delinsCAA ENSP00000514855.1:n.*239_*241delinsCAA
ENST00000380152.8:c.460_462delinsCAA MANE Select ENSP00000369497.3:p.Gln154=
ENST00000544455.6:c.460_462delinsCAA ENSP00000439902.1:p.Gln154=
ENST00000614259.2:c.460_462delinsCAA ENSP00000506251.1:p.Gln154=
ENST00000680887.1:c.460_462delinsCAA ENSP00000505508.1:p.Gln154=
ENST00000380152.7:c.460_462delinsCAA ENSP00000369497.3:p.Gln154=
ENST00000530893.6:n.658_660delinsCAA
ENST00000544455.5:c.460_462delinsCAA ENSP00000439902.1:p.Gln154=
ENST00000614259.1:n.460_462delinsCAA
NM_000059.3:c.460_462delinsCAA , LRG_293t1:c.460_462delinsCAA NP_000050.2:p.Gln154=
XM_011535203.1:c.460_462delinsCAA XP_011533505.1:p.Gln154=
XM_011535204.1:c.460_462delinsCAA XP_011533506.1:p.Gln154=
XM_011535205.1:c.460_462delinsCAA XP_011533507.1:p.Gln154=
NM_000059.4:c.460_462delinsCAA MANE Select NP_000050.3:p.Gln154=