Canonical Allele Identifier: CA2988659073
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162825_43162826insAGTGGCTGCCGCCGCCCCACTGAC , CM000684.2:g.43162825_43162826insAGTGGCTGCCGCCGCCCCACTGAC GRCh38
NC_000022.10:g.43558831_43558832insAGTGGCTGCCGCCGCCCCACTGAC , CM000684.1:g.43558831_43558832insAGTGGCTGCCGCCGCCCCACTGAC GRCh37
NC_000022.9:g.41888775_41888776insAGTGGCTGCCGCCGCCCCACTGAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.344_345insAGTGGCTGCCGCCGCCCCACTGAC MANE Select ENSP00000338004.3:p.Val115_Ser116insValAlaAlaAlaAlaProLeuThr
ENST00000329563.8:c.344_345insAGTGGCTGCCGCCGCCCCACTGAC ENSP00000328973.4:p.Val115_Ser116insValAlaAlaAlaAlaProLeuThr
ENST00000337554.7:c.344_345insAGTGGCTGCCGCCGCCCCACTGAC ENSP00000338004.3:p.Val115_Ser116insValAlaAlaAlaAlaProLeuThr
ENST00000396265.4:c.344_345insAGTGGCTGCCGCCGCCCCACTGAC ENSP00000379563.4:p.Val115_Ser116insValAlaAlaAlaAlaProLeuThr
ENST00000583777.5:c.32_33insAGTGGCTGCCGCCGCCCCACTGAC ENSP00000463495.1:p.Val11_Ser12insValAlaAlaAlaAlaProLeuThr
NM_000714.5:c.344_345insAGTGGCTGCCGCCGCCCCACTGAC NP_000705.2:p.Val115_Ser116insValAlaAlaAlaAlaProLeuThr
NM_001256530.1:c.344_345insAGTGGCTGCCGCCGCCCCACTGAC NP_001243459.1:p.Val115_Ser116insValAlaAlaAlaAlaProLeuThr
NM_001256531.1:c.344_345insAGTGGCTGCCGCCGCCCCACTGAC NP_001243460.1:p.Val115_Ser116insValAlaAlaAlaAlaProLeuThr
NR_046308.1:n.253_254insAGTGGCTGCCGCCGCCCCACTGAC
NM_000714.6:c.344_345insAGTGGCTGCCGCCGCCCCACTGAC MANE Select NP_000705.2:p.Val115_Ser116insValAlaAlaAlaAlaProLeuThr
NR_046308.2:n.208_209insAGTGGCTGCCGCCGCCCCACTGAC