Canonical Allele Identifier: CA2407104132
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162957A= , CM000684.2:g.43162957A= GRCh38
NC_000022.10:g.43558963A= , CM000684.1:g.43558963A= GRCh37
NC_000022.9:g.41888907A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.476A= MANE Select ENSP00000338004.3:p.His159=
ENST00000329563.8:c.476A= ENSP00000328973.4:p.His159=
ENST00000337554.7:c.476A= ENSP00000338004.3:p.His159=
ENST00000396265.4:c.476A= ENSP00000379563.4:p.His159=
ENST00000583777.5:c.164A= ENSP00000463495.1:p.His55=
NM_000714.5:c.476A= NP_000705.2:p.His159=
NM_001256530.1:c.476A= NP_001243459.1:p.His159=
NM_001256531.1:c.476A= NP_001243460.1:p.His159=
NR_046308.1:n.385A=
NM_000714.6:c.476A= MANE Select NP_000705.2:p.His159=
NR_046308.2:n.340A=