Canonical Allele Identifier: CA639829802

Gene: TSPO

Linked Data

• dbSNP Id: rs1433826410
• gnomAD v2: 22-43558882-T-TGGCCGCCCGCC
• gnomAD v3: 22-43162876-T-TGGCCGCCCGCC
• gnomAD v4: 22-43162876-T-TGGCCGCCCGCC
• MyVariant Identifiers: chr22:g.43558882_43558883insGGCCGCCCGCC (hg19) ; chr22:g.43162876_43162877insGGCCGCCCGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162877_43162887dup , CM000684.2:g.43162877_43162887dup	GRCh38
NC_000022.10:g.43558883_43558893dup , CM000684.1:g.43558883_43558893dup	GRCh37
NC_000022.9:g.41888827_41888837dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.396_406dup MANE Select	ENSP00000338004.3:p.Leu136ArgfsTer?
ENST00000329563.8:c.396_406dup	ENSP00000328973.4:p.Leu136ArgfsTer?
ENST00000337554.7:c.396_406dup	ENSP00000338004.3:p.Leu136ArgfsTer?
ENST00000396265.4:c.396_406dup	ENSP00000379563.4:p.Leu136ArgfsTer?
ENST00000583777.5:c.84_94dup	ENSP00000463495.1:p.Leu32ArgfsTer?
NM_000714.5:c.396_406dup	NP_000705.2:p.Leu136ArgfsTer?
NM_001256530.1:c.396_406dup	NP_001243459.1:p.Leu136ArgfsTer?
NM_001256531.1:c.396_406dup	NP_001243460.1:p.Leu136ArgfsTer?
NR_046308.1:n.305_315dup
NM_000714.6:c.396_406dup MANE Select	NP_000705.2:p.Leu136ArgfsTer?
NR_046308.2:n.260_270dup