Canonical Allele Identifier: CA324775921
Gene: TSPO HGNC NCBI

Linked Data

dbSNP Id: rs957157767
gnomAD v2: 22-43558971-C-T
gnomAD v3: 22-43162965-C-T
gnomAD v4: 22-43162965-C-T
COSMIC: COSM5151324 COSM5151325
MyVariant Identifiers: chr22:g.43558971C>T (hg19) chr22:g.43558971_43558974delinsTGTG (hg19) chr22:g.43162965C>T (hg38) chr22:g.43162965_43162968delinsTGTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162965C>T , CM000684.2:g.43162965C>T GRCh38
NC_000022.10:g.43558971C>T , CM000684.1:g.43558971C>T GRCh37
NC_000022.9:g.41888915C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.484C>T MANE Select ENSP00000338004.3:p.Arg162Cys
ENST00000329563.8:c.484C>T ENSP00000328973.4:p.Arg162Cys
ENST00000337554.7:c.484C>T ENSP00000338004.3:p.Arg162Cys
ENST00000396265.4:c.484C>T ENSP00000379563.4:p.Arg162Cys
ENST00000583777.5:c.172C>T ENSP00000463495.1:p.Arg58Cys
NM_000714.5:c.484C>T NP_000705.2:p.Arg162Cys
NM_001256530.1:c.484C>T NP_001243459.1:p.Arg162Cys
NM_001256531.1:c.484C>T NP_001243460.1:p.Arg162Cys
NR_046308.1:n.393C>T
NM_000714.6:c.484C>T MANE Select NP_000705.2:p.Arg162Cys
NR_046308.2:n.348C>T
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