Canonical Allele Identifier: CA2657109567
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162987_43162988del , CM000684.2:g.43162987_43162988del GRCh38
NC_000022.10:g.43558993_43558994del , CM000684.1:g.43558993_43558994del GRCh37
NC_000022.9:g.41888937_41888938del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.506_507del MANE Select ENSP00000338004.3:p.Glu169ValfsTer28
ENST00000329563.8:c.506_507del ENSP00000328973.4:p.Glu169ValfsTer28
ENST00000337554.7:c.506_507del ENSP00000338004.3:p.Glu169ValfsTer28
ENST00000396265.4:c.506_507del ENSP00000379563.4:p.Glu169ValfsTer28
ENST00000583777.5:c.194_195del ENSP00000463495.1:p.Glu65ValfsTer28
NM_000714.5:c.506_507del NP_000705.2:p.Glu169ValfsTer28
NM_001256530.1:c.506_507del NP_001243459.1:p.Glu169ValfsTer28
NM_001256531.1:c.506_507del NP_001243460.1:p.Glu169ValfsTer28
NR_046308.1:n.415_416del
NM_000714.6:c.506_507del MANE Select NP_000705.2:p.Glu169ValfsTer28
NR_046308.2:n.370_371del