Canonical Allele Identifier: CA10272808

Gene: TSPO

Linked Data

• dbSNP Id: rs779133076
• ExAC: 22:43558764 G / A
• gnomAD v2: 22-43558764-G-A
• gnomAD v3: 22-43162758-G-A
• gnomAD v4: 22-43162758-G-A
• MyVariant Identifiers: chr22:g.43558764G>A (hg19) ; chr22:g.43162758G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162758G>A , CM000684.2:g.43162758G>A	GRCh38
NC_000022.10:g.43558764G>A , CM000684.1:g.43558764G>A	GRCh37
NC_000022.9:g.41888708G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.322-45G>A MANE Select	ENSP00000338004.3:n.322-45G>A
ENST00000329563.8:c.322-45G>A	ENSP00000328973.4:n.322-45G>A
ENST00000337554.7:c.322-45G>A	ENSP00000338004.3:n.322-45G>A
ENST00000396265.4:c.322-45G>A	ENSP00000379563.4:n.322-45G>A
ENST00000583777.5:c.10-45G>A	ENSP00000463495.1:n.10-45G>A
NM_000714.5:c.322-45G>A	NP_000705.2:n.322-45G>A
NM_001256530.1:c.322-45G>A	NP_001243459.1:n.322-45G>A
NM_001256531.1:c.322-45G>A	NP_001243460.1:n.322-45G>A
NR_046308.1:n.231-45G>A
NM_000714.6:c.322-45G>A MANE Select	NP_000705.2:n.322-45G>A
NR_046308.2:n.186-45G>A