Canonical Allele Identifier: CA2657109566

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162977-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162979dup , CM000684.2:g.43162979dup	GRCh38
NC_000022.10:g.43558985dup , CM000684.1:g.43558985dup	GRCh37
NC_000022.9:g.41888929dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.498dup MANE Select	ENSP00000338004.3:p.Leu167AlafsTer?
ENST00000329563.8:c.498dup	ENSP00000328973.4:p.Leu167AlafsTer?
ENST00000337554.7:c.498dup	ENSP00000338004.3:p.Leu167AlafsTer?
ENST00000396265.4:c.498dup	ENSP00000379563.4:p.Leu167AlafsTer?
ENST00000583777.5:c.186dup	ENSP00000463495.1:p.Leu63AlafsTer?
NM_000714.5:c.498dup	NP_000705.2:p.Leu167AlafsTer?
NM_001256530.1:c.498dup	NP_001243459.1:p.Leu167AlafsTer?
NM_001256531.1:c.498dup	NP_001243460.1:p.Leu167AlafsTer?
NR_046308.1:n.407dup
NM_000714.6:c.498dup MANE Select	NP_000705.2:p.Leu167AlafsTer?
NR_046308.2:n.362dup