Canonical Allele Identifier: CA411817086
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162920A>C , CM000684.2:g.43162920A>C GRCh38
NC_000022.10:g.43558926A>C , CM000684.1:g.43558926A>C GRCh37
NC_000022.9:g.41888870A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.439A>C MANE Select ENSP00000338004.3:p.Thr147Pro
ENST00000329563.8:c.439A>C ENSP00000328973.4:p.Thr147Pro
ENST00000337554.7:c.439A>C ENSP00000338004.3:p.Thr147Pro
ENST00000396265.4:c.439A>C ENSP00000379563.4:p.Thr147Pro
ENST00000583777.5:c.127A>C ENSP00000463495.1:p.Thr43Pro
NM_000714.5:c.439A>C NP_000705.2:p.Thr147Pro
NM_001256530.1:c.439A>C NP_001243459.1:p.Thr147Pro
NM_001256531.1:c.439A>C NP_001243460.1:p.Thr147Pro
NR_046308.1:n.348A>C
NM_000714.6:c.439A>C MANE Select NP_000705.2:p.Thr147Pro
NR_046308.2:n.303A>C