Canonical Allele Identifier: CA411816909
Gene: TSPO HGNC NCBI

Linked Data

dbSNP Id: rs1369293531

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162831G>A , CM000684.2:g.43162831G>A GRCh38
NC_000022.10:g.43558837G>A , CM000684.1:g.43558837G>A GRCh37
NC_000022.9:g.41888781G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.350G>A MANE Select ENSP00000338004.3:p.Gly117Glu
ENST00000329563.8:c.350G>A ENSP00000328973.4:p.Gly117Glu
ENST00000337554.7:c.350G>A ENSP00000338004.3:p.Gly117Glu
ENST00000396265.4:c.350G>A ENSP00000379563.4:p.Gly117Glu
ENST00000583777.5:c.38G>A ENSP00000463495.1:p.Gly13Glu
NM_000714.5:c.350G>A NP_000705.2:p.Gly117Glu
NM_001256530.1:c.350G>A NP_001243459.1:p.Gly117Glu
NM_001256531.1:c.350G>A NP_001243460.1:p.Gly117Glu
NR_046308.1:n.259G>A
NM_000714.6:c.350G>A MANE Select NP_000705.2:p.Gly117Glu
NR_046308.2:n.214G>A