Canonical Allele Identifier: CA2577740784
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163091G>C , CM000684.2:g.43163091G>C GRCh38
NC_000022.10:g.43559097G>C , CM000684.1:g.43559097G>C GRCh37
NC_000022.9:g.41889041G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*100G>C MANE Select ENSP00000338004.3:n.*100G>C
ENST00000329563.8:c.*100G>C ENSP00000328973.4:n.*100G>C
ENST00000337554.7:c.*100G>C ENSP00000338004.3:n.*100G>C
ENST00000396265.4:c.*100G>C ENSP00000379563.4:n.*100G>C
ENST00000583777.5:c.*100G>C ENSP00000463495.1:n.*100G>C
NM_000714.5:c.*100G>C NP_000705.2:n.*100G>C
NM_001256530.1:c.*100G>C NP_001243459.1:n.*100G>C
NM_001256531.1:c.*100G>C NP_001243460.1:n.*100G>C
NR_046308.1:n.519G>C
NM_000714.6:c.*100G>C MANE Select NP_000705.2:n.*100G>C
NR_046308.2:n.474G>C