Canonical Allele Identifier: CA2819090868
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162894del , CM000684.2:g.43162894del GRCh38
NC_000022.10:g.43558900del , CM000684.1:g.43558900del GRCh37
NC_000022.9:g.41888844del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.413del MANE Select ENSP00000338004.3:p.Tyr138SerfsTer?
ENST00000329563.8:c.413del ENSP00000328973.4:p.Tyr138SerfsTer?
ENST00000337554.7:c.413del ENSP00000338004.3:p.Tyr138SerfsTer?
ENST00000396265.4:c.413del ENSP00000379563.4:p.Tyr138SerfsTer?
ENST00000583777.5:c.101del ENSP00000463495.1:p.Tyr34SerfsTer?
NM_000714.5:c.413del NP_000705.2:p.Tyr138SerfsTer?
NM_001256530.1:c.413del NP_001243459.1:p.Tyr138SerfsTer?
NM_001256531.1:c.413del NP_001243460.1:p.Tyr138SerfsTer?
NR_046308.1:n.322del
NM_000714.6:c.413del MANE Select NP_000705.2:p.Tyr138SerfsTer?
NR_046308.2:n.277del