Canonical Allele Identifier: CA1139772264

Gene: TSPO

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162920A= , CM000684.2:g.43162920A=	GRCh38
NC_000022.10:g.43558926A= , CM000684.1:g.43558926A=	GRCh37
NC_000022.9:g.41888870A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.439A= MANE Select	ENSP00000338004.3:p.Thr147=
ENST00000329563.8:c.439A=	ENSP00000328973.4:p.Thr147=
ENST00000337554.7:c.439A=	ENSP00000338004.3:p.Thr147=
ENST00000396265.4:c.439A=	ENSP00000379563.4:p.Thr147=
ENST00000583777.5:c.127A=	ENSP00000463495.1:p.Thr43=
NM_000714.5:c.439A=	NP_000705.2:p.Thr147=
NM_001256530.1:c.439A=	NP_001243459.1:p.Thr147=
NM_001256531.1:c.439A=	NP_001243460.1:p.Thr147=
NR_046308.1:n.348A=
NM_000714.6:c.439A= MANE Select	NP_000705.2:p.Thr147=
NR_046308.2:n.303A=