Canonical Allele Identifier: CA2739762146
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163049T>A , CM000684.2:g.43163049T>A GRCh38
NC_000022.10:g.43559055T>A , CM000684.1:g.43559055T>A GRCh37
NC_000022.9:g.41888999T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*58T>A MANE Select ENSP00000338004.3:n.*58T>A
ENST00000329563.8:c.*58T>A ENSP00000328973.4:n.*58T>A
ENST00000337554.7:c.*58T>A ENSP00000338004.3:n.*58T>A
ENST00000396265.4:c.*58T>A ENSP00000379563.4:n.*58T>A
ENST00000583777.5:c.*58T>A ENSP00000463495.1:n.*58T>A
NM_000714.5:c.*58T>A NP_000705.2:n.*58T>A
NM_001256530.1:c.*58T>A NP_001243459.1:n.*58T>A
NM_001256531.1:c.*58T>A NP_001243460.1:n.*58T>A
NR_046308.1:n.477T>A
NM_000714.6:c.*58T>A MANE Select NP_000705.2:n.*58T>A
NR_046308.2:n.432T>A