Canonical Allele Identifier: CA514828354

Gene: TSPO

Linked Data

• dbSNP Id: rs755909339
• gnomAD v2: 22-43558841-G-T
• gnomAD v4: 22-43162835-G-T
• MyVariant Identifiers: chr22:g.43558841G>T (hg19) ; chr22:g.43162835G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162835G>T , CM000684.2:g.43162835G>T	GRCh38
NC_000022.10:g.43558841G>T , CM000684.1:g.43558841G>T	GRCh37
NC_000022.9:g.41888785G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.354G>T MANE Select	ENSP00000338004.3:p.Ala118=
ENST00000329563.8:c.354G>T	ENSP00000328973.4:p.Ala118=
ENST00000337554.7:c.354G>T	ENSP00000338004.3:p.Ala118=
ENST00000396265.4:c.354G>T	ENSP00000379563.4:p.Ala118=
ENST00000583777.5:c.42G>T	ENSP00000463495.1:p.Ala14=
NM_000714.5:c.354G>T	NP_000705.2:p.Ala118=
NM_001256530.1:c.354G>T	NP_001243459.1:p.Ala118=
NM_001256531.1:c.354G>T	NP_001243460.1:p.Ala118=
NR_046308.1:n.263G>T
NM_000714.6:c.354G>T MANE Select	NP_000705.2:p.Ala118=
NR_046308.2:n.218G>T