Canonical Allele Identifier: CA2082829028
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32340280_32340281delinsTG , CM000675.2:g.32340280_32340281delinsTG GRCh38
NC_000013.10:g.32914417_32914418delinsTG , CM000675.1:g.32914417_32914418delinsTG GRCh37
NC_000013.9:g.31812417_31812418delinsTG NCBI36
NG_012772.3:g.29801_29802delinsTG , LRG_293:g.29801_29802delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.5925_5926delinsTG ENSP00000434898.2:p.Cys1975=
ENST00000528762.2:c.5925_5926delinsTG ENSP00000433168.2:p.Cys1975=
ENST00000530893.7:c.5556_5557delinsTG ENSP00000499438.2:p.Cys1852=
ENST00000665585.2:c.5925_5926delinsTG ENSP00000499570.2:p.Cys1975=
ENST00000666593.2:c.5925_5926delinsTG ENSP00000499256.2:p.Cys1975=
ENST00000700202.2:c.5925_5926delinsTG ENSP00000514856.2:p.Cys1975=
ENST00000380152.8:c.5925_5926delinsTG MANE Select ENSP00000369497.3:p.Cys1975=
ENST00000544455.6:c.5925_5926delinsTG ENSP00000439902.1:p.Cys1975=
ENST00000614259.2:c.5925_5926delinsTG ENSP00000506251.1:p.Cys1975=
ENST00000680887.1:c.5925_5926delinsTG ENSP00000505508.1:p.Cys1975=
ENST00000380152.7:c.5925_5926delinsTG ENSP00000369497.3:p.Cys1975=
ENST00000544455.5:c.5925_5926delinsTG ENSP00000439902.1:p.Cys1975=
ENST00000614259.1:n.5925_5926delinsTG
NM_000059.3:c.5925_5926delinsTG , LRG_293t1:c.5925_5926delinsTG NP_000050.2:p.Cys1975=
XM_011535203.1:c.5925_5926delinsTG XP_011533505.1:p.Cys1975=
XM_011535204.1:c.5925_5926delinsTG XP_011533506.1:p.Cys1975=
XM_011535205.1:c.5925_5926delinsTG XP_011533507.1:p.Cys1975=
NM_000059.4:c.5925_5926delinsTG MANE Select NP_000050.3:p.Cys1975=