Canonical Allele Identifier: CA411816934
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162846C>A , CM000684.2:g.43162846C>A GRCh38
NC_000022.10:g.43558852C>A , CM000684.1:g.43558852C>A GRCh37
NC_000022.9:g.41888796C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.365C>A MANE Select ENSP00000338004.3:p.Thr122Asn
ENST00000329563.8:c.365C>A ENSP00000328973.4:p.Thr122Asn
ENST00000337554.7:c.365C>A ENSP00000338004.3:p.Thr122Asn
ENST00000396265.4:c.365C>A ENSP00000379563.4:p.Thr122Asn
ENST00000583777.5:c.53C>A ENSP00000463495.1:p.Thr18Asn
NM_000714.5:c.365C>A NP_000705.2:p.Thr122Asn
NM_001256530.1:c.365C>A NP_001243459.1:p.Thr122Asn
NM_001256531.1:c.365C>A NP_001243460.1:p.Thr122Asn
NR_046308.1:n.274C>A
NM_000714.6:c.365C>A MANE Select NP_000705.2:p.Thr122Asn
NR_046308.2:n.229C>A