Canonical Allele Identifier: CA411817102

Gene: TSPO

Linked Data

• MyVariant Identifiers: chr22:g.43558935C>A (hg19) ; chr22:g.43162929C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162929C>A , CM000684.2:g.43162929C>A	GRCh38
NC_000022.10:g.43558935C>A , CM000684.1:g.43558935C>A	GRCh37
NC_000022.9:g.41888879C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.448C>A MANE Select	ENSP00000338004.3:p.Leu150Ile
ENST00000329563.8:c.448C>A	ENSP00000328973.4:p.Leu150Ile
ENST00000337554.7:c.448C>A	ENSP00000338004.3:p.Leu150Ile
ENST00000396265.4:c.448C>A	ENSP00000379563.4:p.Leu150Ile
ENST00000583777.5:c.136C>A	ENSP00000463495.1:p.Leu46Ile
NM_000714.5:c.448C>A	NP_000705.2:p.Leu150Ile
NM_001256530.1:c.448C>A	NP_001243459.1:p.Leu150Ile
NM_001256531.1:c.448C>A	NP_001243460.1:p.Leu150Ile
NR_046308.1:n.357C>A
NM_000714.6:c.448C>A MANE Select	NP_000705.2:p.Leu150Ile
NR_046308.2:n.312C>A