Canonical Allele Identifier: CA2407104302
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163238C= , CM000684.2:g.43163238C= GRCh38
NC_000022.10:g.43559244C= , CM000684.1:g.43559244C= GRCh37
NC_000022.9:g.41889188C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*247C= MANE Select ENSP00000338004.3:n.*247C=
ENST00000337554.7:c.*247C= ENSP00000338004.3:n.*247C=
ENST00000396265.4:c.*247C= ENSP00000379563.4:n.*247C=
ENST00000583777.5:c.*247C= ENSP00000463495.1:n.*247C=
NM_000714.5:c.*247C= NP_000705.2:n.*247C=
NM_001256530.1:c.*247C= NP_001243459.1:n.*247C=
NM_001256531.1:c.*247C= NP_001243460.1:n.*247C=
NR_046308.1:n.666C=
NM_000714.6:c.*247C= MANE Select NP_000705.2:n.*247C=
NR_046308.2:n.621C=