Canonical Allele Identifier: CA411817008
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162881G>T , CM000684.2:g.43162881G>T GRCh38
NC_000022.10:g.43558887G>T , CM000684.1:g.43558887G>T GRCh37
NC_000022.9:g.41888831G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.400G>T MANE Select ENSP00000338004.3:p.Ala134Ser
ENST00000329563.8:c.400G>T ENSP00000328973.4:p.Ala134Ser
ENST00000337554.7:c.400G>T ENSP00000338004.3:p.Ala134Ser
ENST00000396265.4:c.400G>T ENSP00000379563.4:p.Ala134Ser
ENST00000583777.5:c.88G>T ENSP00000463495.1:p.Ala30Ser
NM_000714.5:c.400G>T NP_000705.2:p.Ala134Ser
NM_001256530.1:c.400G>T NP_001243459.1:p.Ala134Ser
NM_001256531.1:c.400G>T NP_001243460.1:p.Ala134Ser
NR_046308.1:n.309G>T
NM_000714.6:c.400G>T MANE Select NP_000705.2:p.Ala134Ser
NR_046308.2:n.264G>T