Canonical Allele Identifier: CA1026020955

Gene: TSPO

Linked Data

• dbSNP Id: rs1931495279
• gnomAD v3: 22-43162924-CCA-C
• gnomAD v4: 22-43162924-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162928_43162929del , CM000684.2:g.43162928_43162929del	GRCh38
NC_000022.10:g.43558934_43558935del , CM000684.1:g.43558934_43558935del	GRCh37
NC_000022.9:g.41888878_41888879del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.447_448del MANE Select	ENSP00000338004.3:p.Leu150GlnfsTer?
ENST00000329563.8:c.447_448del	ENSP00000328973.4:p.Leu150GlnfsTer?
ENST00000337554.7:c.447_448del	ENSP00000338004.3:p.Leu150GlnfsTer?
ENST00000396265.4:c.447_448del	ENSP00000379563.4:p.Leu150GlnfsTer?
ENST00000583777.5:c.135_136del	ENSP00000463495.1:p.Leu46GlnfsTer?
NM_000714.5:c.447_448del	NP_000705.2:p.Leu150GlnfsTer?
NM_001256530.1:c.447_448del	NP_001243459.1:p.Leu150GlnfsTer?
NM_001256531.1:c.447_448del	NP_001243460.1:p.Leu150GlnfsTer?
NR_046308.1:n.356_357del
NM_000714.6:c.447_448del MANE Select	NP_000705.2:p.Leu150GlnfsTer?
NR_046308.2:n.311_312del