Canonical Allele Identifier: CA411816934

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162846-C-A
• MyVariant Identifiers: chr22:g.43558852C>A (hg19) ; chr22:g.43162846C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162846C>A , CM000684.2:g.43162846C>A	GRCh38
NC_000022.10:g.43558852C>A , CM000684.1:g.43558852C>A	GRCh37
NC_000022.9:g.41888796C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.365C>A MANE Select	ENSP00000338004.3:p.Thr122Asn
ENST00000329563.8:c.365C>A	ENSP00000328973.4:p.Thr122Asn
ENST00000337554.7:c.365C>A	ENSP00000338004.3:p.Thr122Asn
ENST00000396265.4:c.365C>A	ENSP00000379563.4:p.Thr122Asn
ENST00000583777.5:c.53C>A	ENSP00000463495.1:p.Thr18Asn
NM_000714.5:c.365C>A	NP_000705.2:p.Thr122Asn
NM_001256530.1:c.365C>A	NP_001243459.1:p.Thr122Asn
NM_001256531.1:c.365C>A	NP_001243460.1:p.Thr122Asn
NR_046308.1:n.274C>A
NM_000714.6:c.365C>A MANE Select	NP_000705.2:p.Thr122Asn
NR_046308.2:n.229C>A