Canonical Allele Identifier: CA10272841
Gene: TSPO HGNC NCBI

Linked Data

dbSNP Id: rs757578697

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162896C>A , CM000684.2:g.43162896C>A GRCh38
NC_000022.10:g.43558902C>A , CM000684.1:g.43558902C>A GRCh37
NC_000022.9:g.41888846C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.415C>A MANE Select ENSP00000338004.3:p.Pro139Thr
ENST00000329563.8:c.415C>A ENSP00000328973.4:p.Pro139Thr
ENST00000337554.7:c.415C>A ENSP00000338004.3:p.Pro139Thr
ENST00000396265.4:c.415C>A ENSP00000379563.4:p.Pro139Thr
ENST00000583777.5:c.103C>A ENSP00000463495.1:p.Pro35Thr
NM_000714.5:c.415C>A NP_000705.2:p.Pro139Thr
NM_001256530.1:c.415C>A NP_001243459.1:p.Pro139Thr
NM_001256531.1:c.415C>A NP_001243460.1:p.Pro139Thr
NR_046308.1:n.324C>A
NM_000714.6:c.415C>A MANE Select NP_000705.2:p.Pro139Thr
NR_046308.2:n.279C>A