Canonical Allele Identifier: CA2407104065
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162829dup , CM000684.2:g.43162829dup GRCh38
NC_000022.10:g.43558835dup , CM000684.1:g.43558835dup GRCh37
NC_000022.9:g.41888779dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.348dup MANE Select ENSP00000338004.3:p.Gly117TrpfsTer?
ENST00000329563.8:c.348dup ENSP00000328973.4:p.Gly117TrpfsTer?
ENST00000337554.7:c.348dup ENSP00000338004.3:p.Gly117TrpfsTer?
ENST00000396265.4:c.348dup ENSP00000379563.4:p.Gly117TrpfsTer?
ENST00000583777.5:c.36dup ENSP00000463495.1:p.Gly13TrpfsTer?
NM_000714.5:c.348dup NP_000705.2:p.Gly117TrpfsTer?
NM_001256530.1:c.348dup NP_001243459.1:p.Gly117TrpfsTer?
NM_001256531.1:c.348dup NP_001243460.1:p.Gly117TrpfsTer?
NR_046308.1:n.257dup
NM_000714.6:c.348dup MANE Select NP_000705.2:p.Gly117TrpfsTer?
NR_046308.2:n.212dup