Canonical Allele Identifier: CA411817097
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162926A>G , CM000684.2:g.43162926A>G GRCh38
NC_000022.10:g.43558932A>G , CM000684.1:g.43558932A>G GRCh37
NC_000022.9:g.41888876A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.445A>G MANE Select ENSP00000338004.3:p.Thr149Ala
ENST00000329563.8:c.445A>G ENSP00000328973.4:p.Thr149Ala
ENST00000337554.7:c.445A>G ENSP00000338004.3:p.Thr149Ala
ENST00000396265.4:c.445A>G ENSP00000379563.4:p.Thr149Ala
ENST00000583777.5:c.133A>G ENSP00000463495.1:p.Thr45Ala
NM_000714.5:c.445A>G NP_000705.2:p.Thr149Ala
NM_001256530.1:c.445A>G NP_001243459.1:p.Thr149Ala
NM_001256531.1:c.445A>G NP_001243460.1:p.Thr149Ala
NR_046308.1:n.354A>G
NM_000714.6:c.445A>G MANE Select NP_000705.2:p.Thr149Ala
NR_046308.2:n.309A>G