Canonical Allele Identifier: CA2657109558

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162881-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162884dup , CM000684.2:g.43162884dup	GRCh38
NC_000022.10:g.43558890dup , CM000684.1:g.43558890dup	GRCh37
NC_000022.9:g.41888834dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.403dup MANE Select	ENSP00000338004.3:p.Arg135ProfsTer?
ENST00000329563.8:c.403dup	ENSP00000328973.4:p.Arg135ProfsTer?
ENST00000337554.7:c.403dup	ENSP00000338004.3:p.Arg135ProfsTer?
ENST00000396265.4:c.403dup	ENSP00000379563.4:p.Arg135ProfsTer?
ENST00000583777.5:c.91dup	ENSP00000463495.1:p.Arg31ProfsTer?
NM_000714.5:c.403dup	NP_000705.2:p.Arg135ProfsTer?
NM_001256530.1:c.403dup	NP_001243459.1:p.Arg135ProfsTer?
NM_001256531.1:c.403dup	NP_001243460.1:p.Arg135ProfsTer?
NR_046308.1:n.312dup
NM_000714.6:c.403dup MANE Select	NP_000705.2:p.Arg135ProfsTer?
NR_046308.2:n.267dup