Canonical Allele Identifier: CA2082850998
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32354480_32354482delinsAAG , CM000675.2:g.32354480_32354482delinsAAG GRCh38
NC_000013.10:g.32928617_32928619delinsAAG , CM000675.1:g.32928617_32928619delinsAAG GRCh37
NC_000013.9:g.31826617_31826619delinsAAG NCBI36
NG_012772.3:g.44001_44003delinsAAG , LRG_293:g.44001_44003delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7008-381_7008-379delinsAAG ENSP00000434898.2:n.7008-381_7008-379delinsAAG
ENST00000528762.2:c.7008-381_7008-379delinsAAG ENSP00000433168.2:n.7008-381_7008-379delinsAAG
ENST00000530893.7:c.6639-381_6639-379delinsAAG ENSP00000499438.2:n.6639-381_6639-379delinsAAG
ENST00000665585.2:c.7008-381_7008-379delinsAAG ENSP00000499570.2:n.7008-381_7008-379delinsAAG
ENST00000666593.2:c.7008-381_7008-379delinsAAG ENSP00000499256.2:n.7008-381_7008-379delinsAAG
ENST00000700202.2:c.7008-381_7008-379delinsAAG ENSP00000514856.2:n.7008-381_7008-379delinsAAG
ENST00000380152.8:c.7008-381_7008-379delinsAAG MANE Select ENSP00000369497.3:n.7008-381_7008-379delinsAAG
ENST00000544455.6:c.7008-381_7008-379delinsAAG ENSP00000439902.1:n.7008-381_7008-379delinsAAG
ENST00000614259.2:c.7008-381_7008-379delinsAAG ENSP00000506251.1:n.7008-381_7008-379delinsAAG
ENST00000680887.1:c.7008-381_7008-379delinsAAG ENSP00000505508.1:n.7008-381_7008-379delinsAAG
ENST00000380152.7:c.7008-381_7008-379delinsAAG ENSP00000369497.3:n.7008-381_7008-379delinsAAG
ENST00000544455.5:c.7008-381_7008-379delinsAAG ENSP00000439902.1:n.7008-381_7008-379delinsAAG
ENST00000614259.1:n.7008-381_7008-379delinsAAG
NM_000059.3:c.7008-381_7008-379delinsAAG , LRG_293t1:c.7008-381_7008-379delinsAAG NP_000050.2:n.7008-381_7008-379delinsAAG
XM_011535203.1:c.7008-381_7008-379delinsAAG XP_011533505.1:n.7008-381_7008-379delinsAAG
XM_011535204.1:c.6912-381_6912-379delinsAAG XP_011533506.1:n.6912-381_6912-379delinsAAG
XM_011535205.1:c.7008-381_7008-379delinsAAG XP_011533507.1:n.7008-381_7008-379delinsAAG
NM_000059.4:c.7008-381_7008-379delinsAAG MANE Select NP_000050.3:n.7008-381_7008-379delinsAAG