Canonical Allele Identifier: CA411816865
Gene: TSPO HGNC NCBI

Linked Data

dbSNP Id: rs1569481008

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162809G>A , CM000684.2:g.43162809G>A GRCh38
NC_000022.10:g.43558815G>A , CM000684.1:g.43558815G>A GRCh37
NC_000022.9:g.41888759G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.328G>A MANE Select ENSP00000338004.3:p.Val110Met
ENST00000329563.8:c.328G>A ENSP00000328973.4:p.Val110Met
ENST00000337554.7:c.328G>A ENSP00000338004.3:p.Val110Met
ENST00000396265.4:c.328G>A ENSP00000379563.4:p.Val110Met
ENST00000583777.5:c.16G>A ENSP00000463495.1:p.Val6Met
NM_000714.5:c.328G>A NP_000705.2:p.Val110Met
NM_001256530.1:c.328G>A NP_001243459.1:p.Val110Met
NM_001256531.1:c.328G>A NP_001243460.1:p.Val110Met
NR_046308.1:n.237G>A
NM_000714.6:c.328G>A MANE Select NP_000705.2:p.Val110Met
NR_046308.2:n.192G>A