Canonical Allele Identifier: CA411817043
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162900A>T , CM000684.2:g.43162900A>T GRCh38
NC_000022.10:g.43558906A>T , CM000684.1:g.43558906A>T GRCh37
NC_000022.9:g.41888850A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.419A>T MANE Select ENSP00000338004.3:p.Tyr140Phe
ENST00000329563.8:c.419A>T ENSP00000328973.4:p.Tyr140Phe
ENST00000337554.7:c.419A>T ENSP00000338004.3:p.Tyr140Phe
ENST00000396265.4:c.419A>T ENSP00000379563.4:p.Tyr140Phe
ENST00000583777.5:c.107A>T ENSP00000463495.1:p.Tyr36Phe
NM_000714.5:c.419A>T NP_000705.2:p.Tyr140Phe
NM_001256530.1:c.419A>T NP_001243459.1:p.Tyr140Phe
NM_001256531.1:c.419A>T NP_001243460.1:p.Tyr140Phe
NR_046308.1:n.328A>T
NM_000714.6:c.419A>T MANE Select NP_000705.2:p.Tyr140Phe
NR_046308.2:n.283A>T