Canonical Allele Identifier: CA2657109782
Gene: TSPO HGNC NCBI

Linked Data

gnomAD v4: 22-43163162-GT-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163163del , CM000684.2:g.43163163del GRCh38
NC_000022.10:g.43559169del , CM000684.1:g.43559169del GRCh37
NC_000022.9:g.41889113del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*172del MANE Select ENSP00000338004.3:n.*172del
ENST00000329563.8:c.*172del ENSP00000328973.4:n.*172del
ENST00000337554.7:c.*172del ENSP00000338004.3:n.*172del
ENST00000396265.4:c.*172del ENSP00000379563.4:n.*172del
ENST00000583777.5:c.*172del ENSP00000463495.1:n.*172del
NM_000714.5:c.*172del NP_000705.2:n.*172del
NM_001256530.1:c.*172del NP_001243459.1:n.*172del
NM_001256531.1:c.*172del NP_001243460.1:n.*172del
NR_046308.1:n.591del
NM_000714.6:c.*172del MANE Select NP_000705.2:n.*172del
NR_046308.2:n.546del
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