Canonical Allele Identifier: CA2657109486
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162745C>G , CM000684.2:g.43162745C>G GRCh38
NC_000022.10:g.43558751C>G , CM000684.1:g.43558751C>G GRCh37
NC_000022.9:g.41888695C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.322-58C>G MANE Select ENSP00000338004.3:n.322-58C>G
ENST00000329563.8:c.322-58C>G ENSP00000328973.4:n.322-58C>G
ENST00000337554.7:c.322-58C>G ENSP00000338004.3:n.322-58C>G
ENST00000396265.4:c.322-58C>G ENSP00000379563.4:n.322-58C>G
ENST00000583777.5:c.10-58C>G ENSP00000463495.1:n.10-58C>G
NM_000714.5:c.322-58C>G NP_000705.2:n.322-58C>G
NM_001256530.1:c.322-58C>G NP_001243459.1:n.322-58C>G
NM_001256531.1:c.322-58C>G NP_001243460.1:n.322-58C>G
NR_046308.1:n.231-58C>G
NM_000714.6:c.322-58C>G MANE Select NP_000705.2:n.322-58C>G
NR_046308.2:n.186-58C>G