Canonical Allele Identifier: CA2407104126
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162944_43162945delinsTG , CM000684.2:g.43162944_43162945delinsTG GRCh38
NC_000022.10:g.43558950_43558951delinsTG , CM000684.1:g.43558950_43558951delinsTG GRCh37
NC_000022.9:g.41888894_41888895delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.463_464delinsTG MANE Select ENSP00000338004.3:p.Trp155=
ENST00000329563.8:c.463_464delinsTG ENSP00000328973.4:p.Trp155=
ENST00000337554.7:c.463_464delinsTG ENSP00000338004.3:p.Trp155=
ENST00000396265.4:c.463_464delinsTG ENSP00000379563.4:p.Trp155=
ENST00000583777.5:c.151_152delinsTG ENSP00000463495.1:p.Trp51=
NM_000714.5:c.463_464delinsTG NP_000705.2:p.Trp155=
NM_001256530.1:c.463_464delinsTG NP_001243459.1:p.Trp155=
NM_001256531.1:c.463_464delinsTG NP_001243460.1:p.Trp155=
NR_046308.1:n.372_373delinsTG
NM_000714.6:c.463_464delinsTG MANE Select NP_000705.2:p.Trp155=
NR_046308.2:n.327_328delinsTG