Canonical Allele Identifier: CA411816881
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162816T>A , CM000684.2:g.43162816T>A GRCh38
NC_000022.10:g.43558822T>A , CM000684.1:g.43558822T>A GRCh37
NC_000022.9:g.41888766T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.335T>A MANE Select ENSP00000338004.3:p.Leu112His
ENST00000329563.8:c.335T>A ENSP00000328973.4:p.Leu112His
ENST00000337554.7:c.335T>A ENSP00000338004.3:p.Leu112His
ENST00000396265.4:c.335T>A ENSP00000379563.4:p.Leu112His
ENST00000583777.5:c.23T>A ENSP00000463495.1:p.Leu8His
NM_000714.5:c.335T>A NP_000705.2:p.Leu112His
NM_001256530.1:c.335T>A NP_001243459.1:p.Leu112His
NM_001256531.1:c.335T>A NP_001243460.1:p.Leu112His
NR_046308.1:n.244T>A
NM_000714.6:c.335T>A MANE Select NP_000705.2:p.Leu112His
NR_046308.2:n.199T>A