Canonical Allele Identifier: CA753375499

Gene: TSPO

Linked Data

• dbSNP Id: rs1441196288
• gnomAD v3: 22-43163036-C-G
• gnomAD v4: 22-43163036-C-G
• MyVariant Identifiers: chr22:g.43559042C>G (hg19) ; chr22:g.43163036C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163036C>G , CM000684.2:g.43163036C>G	GRCh38
NC_000022.10:g.43559042C>G , CM000684.1:g.43559042C>G	GRCh37
NC_000022.9:g.41888986C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*45C>G MANE Select	ENSP00000338004.3:n.*45C>G
ENST00000329563.8:c.*45C>G	ENSP00000328973.4:n.*45C>G
ENST00000337554.7:c.*45C>G	ENSP00000338004.3:n.*45C>G
ENST00000396265.4:c.*45C>G	ENSP00000379563.4:n.*45C>G
ENST00000583777.5:c.*45C>G	ENSP00000463495.1:n.*45C>G
NM_000714.5:c.*45C>G	NP_000705.2:n.*45C>G
NM_001256530.1:c.*45C>G	NP_001243459.1:n.*45C>G
NM_001256531.1:c.*45C>G	NP_001243460.1:n.*45C>G
NR_046308.1:n.464C>G
NM_000714.6:c.*45C>G MANE Select	NP_000705.2:n.*45C>G
NR_046308.2:n.419C>G