Canonical Allele Identifier: CA411816906
Gene: TSPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162830G>T , CM000684.2:g.43162830G>T GRCh38
NC_000022.10:g.43558836G>T , CM000684.1:g.43558836G>T GRCh37
NC_000022.9:g.41888780G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.349G>T MANE Select ENSP00000338004.3:p.Gly117Trp
ENST00000329563.8:c.349G>T ENSP00000328973.4:p.Gly117Trp
ENST00000337554.7:c.349G>T ENSP00000338004.3:p.Gly117Trp
ENST00000396265.4:c.349G>T ENSP00000379563.4:p.Gly117Trp
ENST00000583777.5:c.37G>T ENSP00000463495.1:p.Gly13Trp
NM_000714.5:c.349G>T NP_000705.2:p.Gly117Trp
NM_001256530.1:c.349G>T NP_001243459.1:p.Gly117Trp
NM_001256531.1:c.349G>T NP_001243460.1:p.Gly117Trp
NR_046308.1:n.258G>T
NM_000714.6:c.349G>T MANE Select NP_000705.2:p.Gly117Trp
NR_046308.2:n.213G>T