Canonical Allele Identifier: CA411816911

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162833-G-C
• MyVariant Identifiers: chr22:g.43558839G>C (hg19) ; chr22:g.43162833G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162833G>C , CM000684.2:g.43162833G>C	GRCh38
NC_000022.10:g.43558839G>C , CM000684.1:g.43558839G>C	GRCh37
NC_000022.9:g.41888783G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.352G>C MANE Select	ENSP00000338004.3:p.Ala118Pro
ENST00000329563.8:c.352G>C	ENSP00000328973.4:p.Ala118Pro
ENST00000337554.7:c.352G>C	ENSP00000338004.3:p.Ala118Pro
ENST00000396265.4:c.352G>C	ENSP00000379563.4:p.Ala118Pro
ENST00000583777.5:c.40G>C	ENSP00000463495.1:p.Ala14Pro
NM_000714.5:c.352G>C	NP_000705.2:p.Ala118Pro
NM_001256530.1:c.352G>C	NP_001243459.1:p.Ala118Pro
NM_001256531.1:c.352G>C	NP_001243460.1:p.Ala118Pro
NR_046308.1:n.261G>C
NM_000714.6:c.352G>C MANE Select	NP_000705.2:p.Ala118Pro
NR_046308.2:n.216G>C