Canonical Allele Identifier: CA411816865

Gene: TSPO

Linked Data

• dbSNP Id: rs1569481008
• gnomAD v4: 22-43162809-G-A
• MyVariant Identifiers: chr22:g.43558815G>A (hg19) ; chr22:g.43162809G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162809G>A , CM000684.2:g.43162809G>A	GRCh38
NC_000022.10:g.43558815G>A , CM000684.1:g.43558815G>A	GRCh37
NC_000022.9:g.41888759G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.328G>A MANE Select	ENSP00000338004.3:p.Val110Met
ENST00000329563.8:c.328G>A	ENSP00000328973.4:p.Val110Met
ENST00000337554.7:c.328G>A	ENSP00000338004.3:p.Val110Met
ENST00000396265.4:c.328G>A	ENSP00000379563.4:p.Val110Met
ENST00000583777.5:c.16G>A	ENSP00000463495.1:p.Val6Met
NM_000714.5:c.328G>A	NP_000705.2:p.Val110Met
NM_001256530.1:c.328G>A	NP_001243459.1:p.Val110Met
NM_001256531.1:c.328G>A	NP_001243460.1:p.Val110Met
NR_046308.1:n.237G>A
NM_000714.6:c.328G>A MANE Select	NP_000705.2:p.Val110Met
NR_046308.2:n.192G>A