Canonical Allele Identifier: CA10272826

Gene: TSPO

Linked Data

• dbSNP Id: rs745897744
• ExAC: 22:43558847 A / C
• gnomAD v2: 22-43558847-A-C
• gnomAD v4: 22-43162841-A-C
• MyVariant Identifiers: chr22:g.43558847A>C (hg19) ; chr22:g.43162841A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162841A>C , CM000684.2:g.43162841A>C	GRCh38
NC_000022.10:g.43558847A>C , CM000684.1:g.43558847A>C	GRCh37
NC_000022.9:g.41888791A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.360A>C MANE Select	ENSP00000338004.3:p.Ala120=
ENST00000329563.8:c.360A>C	ENSP00000328973.4:p.Ala120=
ENST00000337554.7:c.360A>C	ENSP00000338004.3:p.Ala120=
ENST00000396265.4:c.360A>C	ENSP00000379563.4:p.Ala120=
ENST00000583777.5:c.48A>C	ENSP00000463495.1:p.Ala16=
NM_000714.5:c.360A>C	NP_000705.2:p.Ala120=
NM_001256530.1:c.360A>C	NP_001243459.1:p.Ala120=
NM_001256531.1:c.360A>C	NP_001243460.1:p.Ala120=
NR_046308.1:n.269A>C
NM_000714.6:c.360A>C MANE Select	NP_000705.2:p.Ala120=
NR_046308.2:n.224A>C