Canonical Allele Identifier: CA2082769409
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32333072_32333077delinsGAAACT , CM000675.2:g.32333072_32333077delinsGAAACT GRCh38
NC_000013.10:g.32907209_32907214delinsGAAACT , CM000675.1:g.32907209_32907214delinsGAAACT GRCh37
NC_000013.9:g.31805209_31805214delinsGAAACT NCBI36
NG_012772.3:g.22593_22598delinsGAAACT , LRG_293:g.22593_22598delinsGAAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.1594_1599delinsGAAACT ENSP00000434898.2:p.Glu532=
ENST00000528762.2:c.1594_1599delinsGAAACT ENSP00000433168.2:p.Glu532=
ENST00000530893.7:c.1225_1230delinsGAAACT ENSP00000499438.2:p.Glu409=
ENST00000665585.2:c.1594_1599delinsGAAACT ENSP00000499570.2:p.Glu532=
ENST00000666593.2:c.1594_1599delinsGAAACT ENSP00000499256.2:p.Glu532=
ENST00000700202.2:c.1594_1599delinsGAAACT ENSP00000514856.2:p.Glu532=
ENST00000700201.1:c.*1373_*1378delinsGAAACT ENSP00000514855.1:n.*1373_*1378delinsGAAACT
ENST00000380152.8:c.1594_1599delinsGAAACT MANE Select ENSP00000369497.3:p.Glu532=
ENST00000544455.6:c.1594_1599delinsGAAACT ENSP00000439902.1:p.Glu532=
ENST00000614259.2:c.1594_1599delinsGAAACT ENSP00000506251.1:p.Glu532=
ENST00000680887.1:c.1594_1599delinsGAAACT ENSP00000505508.1:p.Glu532=
ENST00000380152.7:c.1594_1599delinsGAAACT ENSP00000369497.3:p.Glu532=
ENST00000530893.6:n.1792_1797delinsGAAACT
ENST00000544455.5:c.1594_1599delinsGAAACT ENSP00000439902.1:p.Glu532=
ENST00000614259.1:n.1594_1599delinsGAAACT
NM_000059.3:c.1594_1599delinsGAAACT , LRG_293t1:c.1594_1599delinsGAAACT NP_000050.2:p.Glu532=
XM_011535203.1:c.1594_1599delinsGAAACT XP_011533505.1:p.Glu532=
XM_011535204.1:c.1594_1599delinsGAAACT XP_011533506.1:p.Glu532=
XM_011535205.1:c.1594_1599delinsGAAACT XP_011533507.1:p.Glu532=
NM_000059.4:c.1594_1599delinsGAAACT MANE Select NP_000050.3:p.Glu532=