Canonical Allele Identifier: CA514828417

Gene: TSPO

Linked Data

• dbSNP Id: rs1232653600
• gnomAD v3: 22-43162928-A-G
• gnomAD v4: 22-43162928-A-G
• MyVariant Identifiers: chr22:g.43558934A>G (hg19) ; chr22:g.43162928A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162928A>G , CM000684.2:g.43162928A>G	GRCh38
NC_000022.10:g.43558934A>G , CM000684.1:g.43558934A>G	GRCh37
NC_000022.9:g.41888878A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.447A>G MANE Select	ENSP00000338004.3:p.Thr149=
ENST00000329563.8:c.447A>G	ENSP00000328973.4:p.Thr149=
ENST00000337554.7:c.447A>G	ENSP00000338004.3:p.Thr149=
ENST00000396265.4:c.447A>G	ENSP00000379563.4:p.Thr149=
ENST00000583777.5:c.135A>G	ENSP00000463495.1:p.Thr45=
NM_000714.5:c.447A>G	NP_000705.2:p.Thr149=
NM_001256530.1:c.447A>G	NP_001243459.1:p.Thr149=
NM_001256531.1:c.447A>G	NP_001243460.1:p.Thr149=
NR_046308.1:n.356A>G
NM_000714.6:c.447A>G MANE Select	NP_000705.2:p.Thr149=
NR_046308.2:n.311A>G