Canonical Allele Identifier: CA2407104292
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163221_43163222delinsAT , CM000684.2:g.43163221_43163222delinsAT GRCh38
NC_000022.10:g.43559227_43559228delinsAT , CM000684.1:g.43559227_43559228delinsAT GRCh37
NC_000022.9:g.41889171_41889172delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*230_*231delinsAT MANE Select ENSP00000338004.3:n.*230_*231delinsAT
ENST00000337554.7:c.*230_*231delinsAT ENSP00000338004.3:n.*230_*231delinsAT
ENST00000396265.4:c.*230_*231delinsAT ENSP00000379563.4:n.*230_*231delinsAT
ENST00000583777.5:c.*230_*231delinsAT ENSP00000463495.1:n.*230_*231delinsAT
NM_000714.5:c.*230_*231delinsAT NP_000705.2:n.*230_*231delinsAT
NM_001256530.1:c.*230_*231delinsAT NP_001243459.1:n.*230_*231delinsAT
NM_001256531.1:c.*230_*231delinsAT NP_001243460.1:n.*230_*231delinsAT
NR_046308.1:n.649_650delinsAT
NM_000714.6:c.*230_*231delinsAT MANE Select NP_000705.2:n.*230_*231delinsAT
NR_046308.2:n.604_605delinsAT