Canonical Allele Identifier: CA514828359
Gene: TSPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.43558847A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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