Canonical Allele Identifier: CA2082811443
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32337156_32337157delinsGT , CM000675.2:g.32337156_32337157delinsGT GRCh38
NC_000013.10:g.32911293_32911294delinsGT , CM000675.1:g.32911293_32911294delinsGT GRCh37
NC_000013.9:g.31809293_31809294delinsGT NCBI36
NG_012772.3:g.26677_26678delinsGT , LRG_293:g.26677_26678delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.2801_2802delinsGT ENSP00000434898.2:p.Gly934=
ENST00000528762.2:c.2801_2802delinsGT ENSP00000433168.2:p.Gly934=
ENST00000530893.7:c.2432_2433delinsGT ENSP00000499438.2:p.Gly811=
ENST00000665585.2:c.2801_2802delinsGT ENSP00000499570.2:p.Gly934=
ENST00000666593.2:c.2801_2802delinsGT ENSP00000499256.2:p.Gly934=
ENST00000700202.2:c.2801_2802delinsGT ENSP00000514856.2:p.Gly934=
ENST00000380152.8:c.2801_2802delinsGT MANE Select ENSP00000369497.3:p.Gly934=
ENST00000544455.6:c.2801_2802delinsGT ENSP00000439902.1:p.Gly934=
ENST00000614259.2:c.2801_2802delinsGT ENSP00000506251.1:p.Gly934=
ENST00000680887.1:c.2801_2802delinsGT ENSP00000505508.1:p.Gly934=
ENST00000380152.7:c.2801_2802delinsGT ENSP00000369497.3:p.Gly934=
ENST00000544455.5:c.2801_2802delinsGT ENSP00000439902.1:p.Gly934=
ENST00000614259.1:n.2801_2802delinsGT
NM_000059.3:c.2801_2802delinsGT , LRG_293t1:c.2801_2802delinsGT NP_000050.2:p.Gly934=
XM_011535203.1:c.2801_2802delinsGT XP_011533505.1:p.Gly934=
XM_011535204.1:c.2801_2802delinsGT XP_011533506.1:p.Gly934=
XM_011535205.1:c.2801_2802delinsGT XP_011533507.1:p.Gly934=
NM_000059.4:c.2801_2802delinsGT MANE Select NP_000050.3:p.Gly934=