Canonical Allele Identifier: CA411817140
Gene: TSPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.43558951G>C (hg19) chr22:g.43162945G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162945G>C , CM000684.2:g.43162945G>C GRCh38
NC_000022.10:g.43558951G>C , CM000684.1:g.43558951G>C GRCh37
NC_000022.9:g.41888895G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.464G>C MANE Select ENSP00000338004.3:p.Trp155Ser
ENST00000329563.8:c.464G>C ENSP00000328973.4:p.Trp155Ser
ENST00000337554.7:c.464G>C ENSP00000338004.3:p.Trp155Ser
ENST00000396265.4:c.464G>C ENSP00000379563.4:p.Trp155Ser
ENST00000583777.5:c.152G>C ENSP00000463495.1:p.Trp51Ser
NM_000714.5:c.464G>C NP_000705.2:p.Trp155Ser
NM_001256530.1:c.464G>C NP_001243459.1:p.Trp155Ser
NM_001256531.1:c.464G>C NP_001243460.1:p.Trp155Ser
NR_046308.1:n.373G>C
NM_000714.6:c.464G>C MANE Select NP_000705.2:p.Trp155Ser
NR_046308.2:n.328G>C
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