Canonical Allele Identifier: CA2407104301
Gene: TSPO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163237_43163241delinsCCTTT , CM000684.2:g.43163237_43163241delinsCCTTT GRCh38
NC_000022.10:g.43559243_43559247delinsCCTTT , CM000684.1:g.43559243_43559247delinsCCTTT GRCh37
NC_000022.9:g.41889187_41889191delinsCCTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*246_*250delinsCCTTT MANE Select ENSP00000338004.3:n.*246_*250delinsCCTTT
ENST00000337554.7:c.*246_*250delinsCCTTT ENSP00000338004.3:n.*246_*250delinsCCTTT
ENST00000396265.4:c.*246_*250delinsCCTTT ENSP00000379563.4:n.*246_*250delinsCCTTT
ENST00000583777.5:c.*246_*250delinsCCTTT ENSP00000463495.1:n.*246_*250delinsCCTTT
NM_000714.5:c.*246_*250delinsCCTTT NP_000705.2:n.*246_*250delinsCCTTT
NM_001256530.1:c.*246_*250delinsCCTTT NP_001243459.1:n.*246_*250delinsCCTTT
NM_001256531.1:c.*246_*250delinsCCTTT NP_001243460.1:n.*246_*250delinsCCTTT
NR_046308.1:n.665_669delinsCCTTT
NM_000714.6:c.*246_*250delinsCCTTT MANE Select NP_000705.2:n.*246_*250delinsCCTTT
NR_046308.2:n.620_624delinsCCTTT
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