Canonical Allele Identifier: CA2657109559

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162920-A-ACCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162921_43162922insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC , CM000684.2:g.43162921_43162922insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	GRCh38
NC_000022.10:g.43558927_43558928insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC , CM000684.1:g.43558927_43558928insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	GRCh37
NC_000022.9:g.41888871_41888872insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.440_441insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC MANE Select	ENSP00000338004.3:p.Thr149LeufsTer?
ENST00000329563.8:c.440_441insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	ENSP00000328973.4:p.Thr149LeufsTer?
ENST00000337554.7:c.440_441insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	ENSP00000338004.3:p.Thr149LeufsTer?
ENST00000396265.4:c.440_441insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	ENSP00000379563.4:p.Thr149LeufsTer?
ENST00000583777.5:c.128_129insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	ENSP00000463495.1:p.Thr45LeufsTer?
NM_000714.5:c.440_441insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	NP_000705.2:p.Thr149LeufsTer?
NM_001256530.1:c.440_441insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	NP_001243459.1:p.Thr149LeufsTer?
NM_001256531.1:c.440_441insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC	NP_001243460.1:p.Thr149LeufsTer?
NR_046308.1:n.349_350insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC
NM_000714.6:c.440_441insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC MANE Select	NP_000705.2:p.Thr149LeufsTer?
NR_046308.2:n.304_305insCACACTCAACTACTGCGTATGGCGGGACAACCTACCTGGCCTGGCTGGCCTTCGC