Canonical Allele Identifier: CA411816914
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162834C>G , CM000684.2:g.43162834C>G GRCh38
NC_000022.10:g.43558840C>G , CM000684.1:g.43558840C>G GRCh37
NC_000022.9:g.41888784C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.353C>G MANE Select ENSP00000338004.3:p.Ala118Gly
ENST00000329563.8:c.353C>G ENSP00000328973.4:p.Ala118Gly
ENST00000337554.7:c.353C>G ENSP00000338004.3:p.Ala118Gly
ENST00000396265.4:c.353C>G ENSP00000379563.4:p.Ala118Gly
ENST00000583777.5:c.41C>G ENSP00000463495.1:p.Ala14Gly
NM_000714.5:c.353C>G NP_000705.2:p.Ala118Gly
NM_001256530.1:c.353C>G NP_001243459.1:p.Ala118Gly
NM_001256531.1:c.353C>G NP_001243460.1:p.Ala118Gly
NR_046308.1:n.262C>G
NM_000714.6:c.353C>G MANE Select NP_000705.2:p.Ala118Gly
NR_046308.2:n.217C>G