Canonical Allele Identifier: CA2082827329
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32340127_32340129delinsTCA , CM000675.2:g.32340127_32340129delinsTCA GRCh38
NC_000013.10:g.32914264_32914266delinsTCA , CM000675.1:g.32914264_32914266delinsTCA GRCh37
NC_000013.9:g.31812264_31812266delinsTCA NCBI36
NG_012772.3:g.29648_29650delinsTCA , LRG_293:g.29648_29650delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.5772_5774delinsTCA ENSP00000434898.2:p.Ile1924=
ENST00000528762.2:c.5772_5774delinsTCA ENSP00000433168.2:p.Ile1924=
ENST00000530893.7:c.5403_5405delinsTCA ENSP00000499438.2:p.Ile1801=
ENST00000665585.2:c.5772_5774delinsTCA ENSP00000499570.2:p.Ile1924=
ENST00000666593.2:c.5772_5774delinsTCA ENSP00000499256.2:p.Ile1924=
ENST00000700202.2:c.5772_5774delinsTCA ENSP00000514856.2:p.Ile1924=
ENST00000380152.8:c.5772_5774delinsTCA MANE Select ENSP00000369497.3:p.Ile1924=
ENST00000544455.6:c.5772_5774delinsTCA ENSP00000439902.1:p.Ile1924=
ENST00000614259.2:c.5772_5774delinsTCA ENSP00000506251.1:p.Ile1924=
ENST00000680887.1:c.5772_5774delinsTCA ENSP00000505508.1:p.Ile1924=
ENST00000380152.7:c.5772_5774delinsTCA ENSP00000369497.3:p.Ile1924=
ENST00000544455.5:c.5772_5774delinsTCA ENSP00000439902.1:p.Ile1924=
ENST00000614259.1:n.5772_5774delinsTCA
NM_000059.3:c.5772_5774delinsTCA , LRG_293t1:c.5772_5774delinsTCA NP_000050.2:p.Ile1924=
XM_011535203.1:c.5772_5774delinsTCA XP_011533505.1:p.Ile1924=
XM_011535204.1:c.5772_5774delinsTCA XP_011533506.1:p.Ile1924=
XM_011535205.1:c.5772_5774delinsTCA XP_011533507.1:p.Ile1924=
NM_000059.4:c.5772_5774delinsTCA MANE Select NP_000050.3:p.Ile1924=