Canonical Allele Identifier: CA2657109560

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162958-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162960del , CM000684.2:g.43162960del	GRCh38
NC_000022.10:g.43558966del , CM000684.1:g.43558966del	GRCh37
NC_000022.9:g.41888910del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.479del MANE Select	ENSP00000338004.3:p.Gly160AlafsTer29
ENST00000329563.8:c.479del	ENSP00000328973.4:p.Gly160AlafsTer29
ENST00000337554.7:c.479del	ENSP00000338004.3:p.Gly160AlafsTer29
ENST00000396265.4:c.479del	ENSP00000379563.4:p.Gly160AlafsTer29
ENST00000583777.5:c.167del	ENSP00000463495.1:p.Gly56AlafsTer29
NM_000714.5:c.479del	NP_000705.2:p.Gly160AlafsTer29
NM_001256530.1:c.479del	NP_001243459.1:p.Gly160AlafsTer29
NM_001256531.1:c.479del	NP_001243460.1:p.Gly160AlafsTer29
NR_046308.1:n.388del
NM_000714.6:c.479del MANE Select	NP_000705.2:p.Gly160AlafsTer29
NR_046308.2:n.343del