Canonical Allele Identifier: CA2407104074
Gene: TSPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162840_43162841delinsCA , CM000684.2:g.43162840_43162841delinsCA GRCh38
NC_000022.10:g.43558846_43558847delinsCA , CM000684.1:g.43558846_43558847delinsCA GRCh37
NC_000022.9:g.41888790_41888791delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.359_360delinsCA MANE Select ENSP00000338004.3:p.Ala120=
ENST00000329563.8:c.359_360delinsCA ENSP00000328973.4:p.Ala120=
ENST00000337554.7:c.359_360delinsCA ENSP00000338004.3:p.Ala120=
ENST00000396265.4:c.359_360delinsCA ENSP00000379563.4:p.Ala120=
ENST00000583777.5:c.47_48delinsCA ENSP00000463495.1:p.Ala16=
NM_000714.5:c.359_360delinsCA NP_000705.2:p.Ala120=
NM_001256530.1:c.359_360delinsCA NP_001243459.1:p.Ala120=
NM_001256531.1:c.359_360delinsCA NP_001243460.1:p.Ala120=
NR_046308.1:n.268_269delinsCA
NM_000714.6:c.359_360delinsCA MANE Select NP_000705.2:p.Ala120=
NR_046308.2:n.223_224delinsCA