Canonical Allele Identifier: CA2988659086

Gene: TSPO

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162920_43162921del , CM000684.2:g.43162920_43162921del	GRCh38
NC_000022.10:g.43558926_43558927del , CM000684.1:g.43558926_43558927del	GRCh37
NC_000022.9:g.41888870_41888871del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.439_440del MANE Select	ENSP00000338004.3:p.Thr147AspfsTer?
ENST00000329563.8:c.439_440del	ENSP00000328973.4:p.Thr147AspfsTer?
ENST00000337554.7:c.439_440del	ENSP00000338004.3:p.Thr147AspfsTer?
ENST00000396265.4:c.439_440del	ENSP00000379563.4:p.Thr147AspfsTer?
ENST00000583777.5:c.127_128del	ENSP00000463495.1:p.Thr43AspfsTer?
NM_000714.5:c.439_440del	NP_000705.2:p.Thr147AspfsTer?
NM_001256530.1:c.439_440del	NP_001243459.1:p.Thr147AspfsTer?
NM_001256531.1:c.439_440del	NP_001243460.1:p.Thr147AspfsTer?
NR_046308.1:n.348_349del
NM_000714.6:c.439_440del MANE Select	NP_000705.2:p.Thr147AspfsTer?
NR_046308.2:n.303_304del