Canonical Allele Identifier: CA2407104139
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162970G= , CM000684.2:g.43162970G= GRCh38
NC_000022.10:g.43558976G= , CM000684.1:g.43558976G= GRCh37
NC_000022.9:g.41888920G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.489G= MANE Select ENSP00000338004.3:p.Gly163=
ENST00000329563.8:c.489G= ENSP00000328973.4:p.Gly163=
ENST00000337554.7:c.489G= ENSP00000338004.3:p.Gly163=
ENST00000396265.4:c.489G= ENSP00000379563.4:p.Gly163=
ENST00000583777.5:c.177G= ENSP00000463495.1:p.Gly59=
NM_000714.5:c.489G= NP_000705.2:p.Gly163=
NM_001256530.1:c.489G= NP_001243459.1:p.Gly163=
NM_001256531.1:c.489G= NP_001243460.1:p.Gly163=
NR_046308.1:n.398G=
NM_000714.6:c.489G= MANE Select NP_000705.2:p.Gly163=
NR_046308.2:n.353G=