Canonical Allele Identifier: CA639829803

Gene: TSPO

Linked Data

• dbSNP Id: rs1226700027
• gnomAD v2: 22-43558950-TG-T
• gnomAD v4: 22-43162944-TG-T
• MyVariant Identifiers: chr22:g.43558951del (hg19) ; chr22:g.43162945del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162946del , CM000684.2:g.43162946del	GRCh38
NC_000022.10:g.43558952del , CM000684.1:g.43558952del	GRCh37
NC_000022.9:g.41888896del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.465del MANE Select	ENSP00000338004.3:p.Trp155CysfsTer?
ENST00000329563.8:c.465del	ENSP00000328973.4:p.Trp155CysfsTer?
ENST00000337554.7:c.465del	ENSP00000338004.3:p.Trp155CysfsTer?
ENST00000396265.4:c.465del	ENSP00000379563.4:p.Trp155CysfsTer?
ENST00000583777.5:c.153del	ENSP00000463495.1:p.Trp51CysfsTer?
NM_000714.5:c.465del	NP_000705.2:p.Trp155CysfsTer?
NM_001256530.1:c.465del	NP_001243459.1:p.Trp155CysfsTer?
NM_001256531.1:c.465del	NP_001243460.1:p.Trp155CysfsTer?
NR_046308.1:n.374del
NM_000714.6:c.465del MANE Select	NP_000705.2:p.Trp155CysfsTer?
NR_046308.2:n.329del