Canonical Allele Identifier: CA10272849
Gene: TSPO HGNC NCBI

Linked Data

dbSNP Id: rs748472790

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162922G>A , CM000684.2:g.43162922G>A GRCh38
NC_000022.10:g.43558928G>A , CM000684.1:g.43558928G>A GRCh37
NC_000022.9:g.41888872G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.441G>A MANE Select ENSP00000338004.3:p.Thr147=
ENST00000329563.8:c.441G>A ENSP00000328973.4:p.Thr147=
ENST00000337554.7:c.441G>A ENSP00000338004.3:p.Thr147=
ENST00000396265.4:c.441G>A ENSP00000379563.4:p.Thr147=
ENST00000583777.5:c.129G>A ENSP00000463495.1:p.Thr43=
NM_000714.5:c.441G>A NP_000705.2:p.Thr147=
NM_001256530.1:c.441G>A NP_001243459.1:p.Thr147=
NM_001256531.1:c.441G>A NP_001243460.1:p.Thr147=
NR_046308.1:n.350G>A
NM_000714.6:c.441G>A MANE Select NP_000705.2:p.Thr147=
NR_046308.2:n.305G>A