Canonical Allele Identifier: CA753375167

Gene: TSPO

Linked Data

• dbSNP Id: rs1201860230
• gnomAD v3: 22-43162840-CA-C
• gnomAD v4: 22-43162840-CA-C
• MyVariant Identifiers: chr22:g.43558847del (hg19) ; chr22:g.43162841del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162841del , CM000684.2:g.43162841del	GRCh38
NC_000022.10:g.43558847del , CM000684.1:g.43558847del	GRCh37
NC_000022.9:g.41888791del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.360del MANE Select	ENSP00000338004.3:p.Ala121ProfsTer9
ENST00000329563.8:c.360del	ENSP00000328973.4:p.Ala121ProfsTer9
ENST00000337554.7:c.360del	ENSP00000338004.3:p.Ala121ProfsTer9
ENST00000396265.4:c.360del	ENSP00000379563.4:p.Ala121ProfsTer9
ENST00000583777.5:c.48del	ENSP00000463495.1:p.Ala17ProfsTer9
NM_000714.5:c.360del	NP_000705.2:p.Ala121ProfsTer9
NM_001256530.1:c.360del	NP_001243459.1:p.Ala121ProfsTer9
NM_001256531.1:c.360del	NP_001243460.1:p.Ala121ProfsTer9
NR_046308.1:n.269del
NM_000714.6:c.360del MANE Select	NP_000705.2:p.Ala121ProfsTer9
NR_046308.2:n.224del