Canonical Allele Identifier: CA2407104112
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162919C= , CM000684.2:g.43162919C= GRCh38
NC_000022.10:g.43558925C= , CM000684.1:g.43558925C= GRCh37
NC_000022.9:g.41888869C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.438C= MANE Select ENSP00000338004.3:p.Phe146=
ENST00000329563.8:c.438C= ENSP00000328973.4:p.Phe146=
ENST00000337554.7:c.438C= ENSP00000338004.3:p.Phe146=
ENST00000396265.4:c.438C= ENSP00000379563.4:p.Phe146=
ENST00000583777.5:c.126C= ENSP00000463495.1:p.Phe42=
NM_000714.5:c.438C= NP_000705.2:p.Phe146=
NM_001256530.1:c.438C= NP_001243459.1:p.Phe146=
NM_001256531.1:c.438C= NP_001243460.1:p.Phe146=
NR_046308.1:n.347C=
NM_000714.6:c.438C= MANE Select NP_000705.2:p.Phe146=
NR_046308.2:n.302C=