Canonical Allele Identifier: CA411817212

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162983-C-G
• MyVariant Identifiers: chr22:g.43558989C>G (hg19) ; chr22:g.43162983C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162983C>G , CM000684.2:g.43162983C>G	GRCh38
NC_000022.10:g.43558989C>G , CM000684.1:g.43558989C>G	GRCh37
NC_000022.9:g.41888933C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.502C>G MANE Select	ENSP00000338004.3:p.Pro168Ala
ENST00000329563.8:c.502C>G	ENSP00000328973.4:p.Pro168Ala
ENST00000337554.7:c.502C>G	ENSP00000338004.3:p.Pro168Ala
ENST00000396265.4:c.502C>G	ENSP00000379563.4:p.Pro168Ala
ENST00000583777.5:c.190C>G	ENSP00000463495.1:p.Pro64Ala
NM_000714.5:c.502C>G	NP_000705.2:p.Pro168Ala
NM_001256530.1:c.502C>G	NP_001243459.1:p.Pro168Ala
NM_001256531.1:c.502C>G	NP_001243460.1:p.Pro168Ala
NR_046308.1:n.411C>G
NM_000714.6:c.502C>G MANE Select	NP_000705.2:p.Pro168Ala
NR_046308.2:n.366C>G