Canonical Allele Identifier: CA2657109461
Gene: TSPO HGNC NCBI

Linked Data

gnomAD v4: 22-43162722-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162725del , CM000684.2:g.43162725del GRCh38
NC_000022.10:g.43558731del , CM000684.1:g.43558731del GRCh37
NC_000022.9:g.41888675del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.322-78del MANE Select ENSP00000338004.3:n.322-78del
ENST00000329563.8:c.322-78del ENSP00000328973.4:n.322-78del
ENST00000337554.7:c.322-78del ENSP00000338004.3:n.322-78del
ENST00000396265.4:c.322-78del ENSP00000379563.4:n.322-78del
ENST00000583777.5:c.10-78del ENSP00000463495.1:n.10-78del
NM_000714.5:c.322-78del NP_000705.2:n.322-78del
NM_001256530.1:c.322-78del NP_001243459.1:n.322-78del
NM_001256531.1:c.322-78del NP_001243460.1:n.322-78del
NR_046308.1:n.231-78del
NM_000714.6:c.322-78del MANE Select NP_000705.2:n.322-78del
NR_046308.2:n.186-78del
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