Canonical Allele Identifier: CA2819090869

Gene: TSPO

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162981_43162997del , CM000684.2:g.43162981_43162997del	GRCh38
NC_000022.10:g.43558987_43559003del , CM000684.1:g.43558987_43559003del	GRCh37
NC_000022.9:g.41888931_41888947del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.500_*6del MANE Select	ENSP00000338004.3:n.[c.500_*6del;Leu167ArgfsTer25]
ENST00000329563.8:c.500_*6del	ENSP00000328973.4:n.[c.500_*6del;Leu167ArgfsTer25]
ENST00000337554.7:c.500_*6del	ENSP00000338004.3:n.[c.500_*6del;Leu167ArgfsTer25]
ENST00000396265.4:c.500_*6del	ENSP00000379563.4:n.[c.500_*6del;Leu167ArgfsTer25]
ENST00000583777.5:c.188_*6del	ENSP00000463495.1:n.[c.188_*6del;Leu63ArgfsTer25]
NM_000714.5:c.500_*6del	NP_000705.2:n.[c.500_*6del;Leu167ArgfsTer25]
NM_001256530.1:c.500_*6del	NP_001243459.1:n.[c.500_*6del;Leu167ArgfsTer25]
NM_001256531.1:c.500_*6del	NP_001243460.1:n.[c.500_*6del;Leu167ArgfsTer25]
NR_046308.1:n.409_425del
NM_000714.6:c.500_*6del MANE Select	NP_000705.2:n.[c.500_*6del;Leu167ArgfsTer25]
NR_046308.2:n.364_380del