Canonical Allele Identifier: CA2407104115
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162924_43162926delinsCCA , CM000684.2:g.43162924_43162926delinsCCA GRCh38
NC_000022.10:g.43558930_43558932delinsCCA , CM000684.1:g.43558930_43558932delinsCCA GRCh37
NC_000022.9:g.41888874_41888876delinsCCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.443_445delinsCCA MANE Select ENSP00000338004.3:p.Thr148=
ENST00000329563.8:c.443_445delinsCCA ENSP00000328973.4:p.Thr148=
ENST00000337554.7:c.443_445delinsCCA ENSP00000338004.3:p.Thr148=
ENST00000396265.4:c.443_445delinsCCA ENSP00000379563.4:p.Thr148=
ENST00000583777.5:c.131_133delinsCCA ENSP00000463495.1:p.Thr44=
NM_000714.5:c.443_445delinsCCA NP_000705.2:p.Thr148=
NM_001256530.1:c.443_445delinsCCA NP_001243459.1:p.Thr148=
NM_001256531.1:c.443_445delinsCCA NP_001243460.1:p.Thr148=
NR_046308.1:n.352_354delinsCCA
NM_000714.6:c.443_445delinsCCA MANE Select NP_000705.2:p.Thr148=
NR_046308.2:n.307_309delinsCCA