Canonical Allele Identifier: CA411817117

Gene: TSPO

Linked Data

• MyVariant Identifiers: chr22:g.43558941T>A (hg19) ; chr22:g.43162935T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162935T>A , CM000684.2:g.43162935T>A	GRCh38
NC_000022.10:g.43558941T>A , CM000684.1:g.43558941T>A	GRCh37
NC_000022.9:g.41888885T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.454T>A MANE Select	ENSP00000338004.3:p.Tyr152Asn
ENST00000329563.8:c.454T>A	ENSP00000328973.4:p.Tyr152Asn
ENST00000337554.7:c.454T>A	ENSP00000338004.3:p.Tyr152Asn
ENST00000396265.4:c.454T>A	ENSP00000379563.4:p.Tyr152Asn
ENST00000583777.5:c.142T>A	ENSP00000463495.1:p.Tyr48Asn
NM_000714.5:c.454T>A	NP_000705.2:p.Tyr152Asn
NM_001256530.1:c.454T>A	NP_001243459.1:p.Tyr152Asn
NM_001256531.1:c.454T>A	NP_001243460.1:p.Tyr152Asn
NR_046308.1:n.363T>A
NM_000714.6:c.454T>A MANE Select	NP_000705.2:p.Tyr152Asn
NR_046308.2:n.318T>A