Canonical Allele Identifier: CA411817091

Gene: TSPO

Linked Data

• MyVariant Identifiers: chr22:g.43558929A>G (hg19) ; chr22:g.43162923A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162923A>G , CM000684.2:g.43162923A>G	GRCh38
NC_000022.10:g.43558929A>G , CM000684.1:g.43558929A>G	GRCh37
NC_000022.9:g.41888873A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.442A>G MANE Select	ENSP00000338004.3:p.Thr148Ala
ENST00000329563.8:c.442A>G	ENSP00000328973.4:p.Thr148Ala
ENST00000337554.7:c.442A>G	ENSP00000338004.3:p.Thr148Ala
ENST00000396265.4:c.442A>G	ENSP00000379563.4:p.Thr148Ala
ENST00000583777.5:c.130A>G	ENSP00000463495.1:p.Thr44Ala
NM_000714.5:c.442A>G	NP_000705.2:p.Thr148Ala
NM_001256530.1:c.442A>G	NP_001243459.1:p.Thr148Ala
NM_001256531.1:c.442A>G	NP_001243460.1:p.Thr148Ala
NR_046308.1:n.351A>G
NM_000714.6:c.442A>G MANE Select	NP_000705.2:p.Thr148Ala
NR_046308.2:n.306A>G