Canonical Allele Identifier: CA2407104113
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162921C= , CM000684.2:g.43162921C= GRCh38
NC_000022.10:g.43558927C= , CM000684.1:g.43558927C= GRCh37
NC_000022.9:g.41888871C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.440C= MANE Select ENSP00000338004.3:p.Thr147=
ENST00000329563.8:c.440C= ENSP00000328973.4:p.Thr147=
ENST00000337554.7:c.440C= ENSP00000338004.3:p.Thr147=
ENST00000396265.4:c.440C= ENSP00000379563.4:p.Thr147=
ENST00000583777.5:c.128C= ENSP00000463495.1:p.Thr43=
NM_000714.5:c.440C= NP_000705.2:p.Thr147=
NM_001256530.1:c.440C= NP_001243459.1:p.Thr147=
NM_001256531.1:c.440C= NP_001243460.1:p.Thr147=
NR_046308.1:n.349C=
NM_000714.6:c.440C= MANE Select NP_000705.2:p.Thr147=
NR_046308.2:n.304C=