Canonical Allele Identifier: CA2407104259
Gene: TSPO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163159A= , CM000684.2:g.43163159A= GRCh38
NC_000022.10:g.43559165A= , CM000684.1:g.43559165A= GRCh37
NC_000022.9:g.41889109A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*168A= MANE Select ENSP00000338004.3:n.*168A=
ENST00000329563.8:c.*168A= ENSP00000328973.4:n.*168A=
ENST00000337554.7:c.*168A= ENSP00000338004.3:n.*168A=
ENST00000396265.4:c.*168A= ENSP00000379563.4:n.*168A=
ENST00000583777.5:c.*168A= ENSP00000463495.1:n.*168A=
NM_000714.5:c.*168A= NP_000705.2:n.*168A=
NM_001256530.1:c.*168A= NP_001243459.1:n.*168A=
NM_001256531.1:c.*168A= NP_001243460.1:n.*168A=
NR_046308.1:n.587A=
NM_000714.6:c.*168A= MANE Select NP_000705.2:n.*168A=
NR_046308.2:n.542A=
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