Canonical Allele Identifier: CA2407104122
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162939G= , CM000684.2:g.43162939G= GRCh38
NC_000022.10:g.43558945G= , CM000684.1:g.43558945G= GRCh37
NC_000022.9:g.41888889G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.458G= MANE Select ENSP00000338004.3:p.Cys153=
ENST00000329563.8:c.458G= ENSP00000328973.4:p.Cys153=
ENST00000337554.7:c.458G= ENSP00000338004.3:p.Cys153=
ENST00000396265.4:c.458G= ENSP00000379563.4:p.Cys153=
ENST00000583777.5:c.146G= ENSP00000463495.1:p.Cys49=
NM_000714.5:c.458G= NP_000705.2:p.Cys153=
NM_001256530.1:c.458G= NP_001243459.1:p.Cys153=
NM_001256531.1:c.458G= NP_001243460.1:p.Cys153=
NR_046308.1:n.367G=
NM_000714.6:c.458G= MANE Select NP_000705.2:p.Cys153=
NR_046308.2:n.322G=