Canonical Allele Identifier: CA639829812

Gene: TSPO

Linked Data

• dbSNP Id: rs1427814024
• gnomAD v2: 22-43559033-A-T
• MyVariant Identifiers: chr22:g.43559033A>T (hg19) ; chr22:g.43163027A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163027A>T , CM000684.2:g.43163027A>T	GRCh38
NC_000022.10:g.43559033A>T , CM000684.1:g.43559033A>T	GRCh37
NC_000022.9:g.41888977A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*36A>T MANE Select	ENSP00000338004.3:n.*36A>T
ENST00000329563.8:c.*36A>T	ENSP00000328973.4:n.*36A>T
ENST00000337554.7:c.*36A>T	ENSP00000338004.3:n.*36A>T
ENST00000396265.4:c.*36A>T	ENSP00000379563.4:n.*36A>T
ENST00000583777.5:c.*36A>T	ENSP00000463495.1:n.*36A>T
NM_000714.5:c.*36A>T	NP_000705.2:n.*36A>T
NM_001256530.1:c.*36A>T	NP_001243459.1:n.*36A>T
NM_001256531.1:c.*36A>T	NP_001243460.1:n.*36A>T
NR_046308.1:n.455A>T
NM_000714.6:c.*36A>T MANE Select	NP_000705.2:n.*36A>T
NR_046308.2:n.410A>T