Canonical Allele Identifier: CA411817118

Gene: TSPO

Linked Data

• MyVariant Identifiers: chr22:g.43558942A>C (hg19) ; chr22:g.43162936A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162936A>C , CM000684.2:g.43162936A>C	GRCh38
NC_000022.10:g.43558942A>C , CM000684.1:g.43558942A>C	GRCh37
NC_000022.9:g.41888886A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.455A>C MANE Select	ENSP00000338004.3:p.Tyr152Ser
ENST00000329563.8:c.455A>C	ENSP00000328973.4:p.Tyr152Ser
ENST00000337554.7:c.455A>C	ENSP00000338004.3:p.Tyr152Ser
ENST00000396265.4:c.455A>C	ENSP00000379563.4:p.Tyr152Ser
ENST00000583777.5:c.143A>C	ENSP00000463495.1:p.Tyr48Ser
NM_000714.5:c.455A>C	NP_000705.2:p.Tyr152Ser
NM_001256530.1:c.455A>C	NP_001243459.1:p.Tyr152Ser
NM_001256531.1:c.455A>C	NP_001243460.1:p.Tyr152Ser
NR_046308.1:n.364A>C
NM_000714.6:c.455A>C MANE Select	NP_000705.2:p.Tyr152Ser
NR_046308.2:n.319A>C