Canonical Allele Identifier: CA2819090875

Gene: TSPO

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163161_43163162insAGG , CM000684.2:g.43163161_43163162insAGG	GRCh38
NC_000022.10:g.43559167_43559168insAGG , CM000684.1:g.43559167_43559168insAGG	GRCh37
NC_000022.9:g.41889111_41889112insAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*170_*171insAGG MANE Select	ENSP00000338004.3:n.*170_*171insAGG
ENST00000329563.8:c.*170_*171insAGG	ENSP00000328973.4:n.*170_*171insAGG
ENST00000337554.7:c.*170_*171insAGG	ENSP00000338004.3:n.*170_*171insAGG
ENST00000396265.4:c.*170_*171insAGG	ENSP00000379563.4:n.*170_*171insAGG
ENST00000583777.5:c.*170_*171insAGG	ENSP00000463495.1:n.*170_*171insAGG
NM_000714.5:c.*170_*171insAGG	NP_000705.2:n.*170_*171insAGG
NM_001256530.1:c.*170_*171insAGG	NP_001243459.1:n.*170_*171insAGG
NM_001256531.1:c.*170_*171insAGG	NP_001243460.1:n.*170_*171insAGG
NR_046308.1:n.589_590insAGG
NM_000714.6:c.*170_*171insAGG MANE Select	NP_000705.2:n.*170_*171insAGG
NR_046308.2:n.544_545insAGG