Canonical Allele Identifier: CA514828371
Gene: TSPO HGNC NCBI

Linked Data

gnomAD v4: 22-43162856-C-A
MyVariant Identifiers: chr22:g.43558862C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162856C>A , CM000684.2:g.43162856C>A GRCh38
NC_000022.10:g.43558862C>A , CM000684.1:g.43558862C>A GRCh37
NC_000022.9:g.41888806C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.375C>A MANE Select ENSP00000338004.3:p.Ala125=
ENST00000329563.8:c.375C>A ENSP00000328973.4:p.Ala125=
ENST00000337554.7:c.375C>A ENSP00000338004.3:p.Ala125=
ENST00000396265.4:c.375C>A ENSP00000379563.4:p.Ala125=
ENST00000583777.5:c.63C>A ENSP00000463495.1:p.Ala21=
NM_000714.5:c.375C>A NP_000705.2:p.Ala125=
NM_001256530.1:c.375C>A NP_001243459.1:p.Ala125=
NM_001256531.1:c.375C>A NP_001243460.1:p.Ala125=
NR_046308.1:n.284C>A
NM_000714.6:c.375C>A MANE Select NP_000705.2:p.Ala125=
NR_046308.2:n.239C>A
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