Canonical Allele Identifier: CA920376523

Gene: TSPO

Linked Data

• dbSNP Id: rs1371241051
• gnomAD v4: 22-43163034-ATCACGCTTGTGATGTGGTGGCCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163043_43163065del , CM000684.2:g.43163043_43163065del	GRCh38
NC_000022.10:g.43559049_43559071del , CM000684.1:g.43559049_43559071del	GRCh37
NC_000022.9:g.41888993_41889015del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*52_*74del MANE Select	ENSP00000338004.3:n.*52_*74del
ENST00000329563.8:c.*52_*74del	ENSP00000328973.4:n.*52_*74del
ENST00000337554.7:c.*52_*74del	ENSP00000338004.3:n.*52_*74del
ENST00000396265.4:c.*52_*74del	ENSP00000379563.4:n.*52_*74del
ENST00000583777.5:c.*52_*74del	ENSP00000463495.1:n.*52_*74del
NM_000714.5:c.*52_*74del	NP_000705.2:n.*52_*74del
NM_001256530.1:c.*52_*74del	NP_001243459.1:n.*52_*74del
NM_001256531.1:c.*52_*74del	NP_001243460.1:n.*52_*74del
NR_046308.1:n.471_493del
NM_000714.6:c.*52_*74del MANE Select	NP_000705.2:n.*52_*74del
NR_046308.2:n.426_448del