Canonical Allele Identifier: CA2657109765

Gene: TSPO

Linked Data

• gnomAD v4: 22-43163148-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163149dup , CM000684.2:g.43163149dup	GRCh38
NC_000022.10:g.43559155dup , CM000684.1:g.43559155dup	GRCh37
NC_000022.9:g.41889099dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*158dup MANE Select	ENSP00000338004.3:n.*158dup
ENST00000329563.8:c.*158dup	ENSP00000328973.4:n.*158dup
ENST00000337554.7:c.*158dup	ENSP00000338004.3:n.*158dup
ENST00000396265.4:c.*158dup	ENSP00000379563.4:n.*158dup
ENST00000583777.5:c.*158dup	ENSP00000463495.1:n.*158dup
NM_000714.5:c.*158dup	NP_000705.2:n.*158dup
NM_001256530.1:c.*158dup	NP_001243459.1:n.*158dup
NM_001256531.1:c.*158dup	NP_001243460.1:n.*158dup
NR_046308.1:n.577dup
NM_000714.6:c.*158dup MANE Select	NP_000705.2:n.*158dup
NR_046308.2:n.532dup