Canonical Allele Identifier: CA2832577452
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163148dup , CM000684.2:g.43163148dup GRCh38
NC_000022.10:g.43559154dup , CM000684.1:g.43559154dup GRCh37
NC_000022.9:g.41889098dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*157dup MANE Select ENSP00000338004.3:n.*157dup
ENST00000329563.8:c.*157dup ENSP00000328973.4:n.*157dup
ENST00000337554.7:c.*157dup ENSP00000338004.3:n.*157dup
ENST00000396265.4:c.*157dup ENSP00000379563.4:n.*157dup
ENST00000583777.5:c.*157dup ENSP00000463495.1:n.*157dup
NM_000714.5:c.*157dup NP_000705.2:n.*157dup
NM_001256530.1:c.*157dup NP_001243459.1:n.*157dup
NM_001256531.1:c.*157dup NP_001243460.1:n.*157dup
NR_046308.1:n.576dup
NM_000714.6:c.*157dup MANE Select NP_000705.2:n.*157dup
NR_046308.2:n.531dup