Canonical Allele Identifier: CA411817133
Gene: TSPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.43558948T>A (hg19) chr22:g.43162942T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162942T>A , CM000684.2:g.43162942T>A GRCh38
NC_000022.10:g.43558948T>A , CM000684.1:g.43558948T>A GRCh37
NC_000022.9:g.41888892T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.461T>A MANE Select ENSP00000338004.3:p.Val154Glu
ENST00000329563.8:c.461T>A ENSP00000328973.4:p.Val154Glu
ENST00000337554.7:c.461T>A ENSP00000338004.3:p.Val154Glu
ENST00000396265.4:c.461T>A ENSP00000379563.4:p.Val154Glu
ENST00000583777.5:c.149T>A ENSP00000463495.1:p.Val50Glu
NM_000714.5:c.461T>A NP_000705.2:p.Val154Glu
NM_001256530.1:c.461T>A NP_001243459.1:p.Val154Glu
NM_001256531.1:c.461T>A NP_001243460.1:p.Val154Glu
NR_046308.1:n.370T>A
NM_000714.6:c.461T>A MANE Select NP_000705.2:p.Val154Glu
NR_046308.2:n.325T>A
Search 100 bp 5'
Search 100 bp 3'