Canonical Allele Identifier: CA1139772266

Gene: TSPO

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163131G= , CM000684.2:g.43163131G=	GRCh38
NC_000022.10:g.43559137G= , CM000684.1:g.43559137G=	GRCh37
NC_000022.9:g.41889081G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*140G= MANE Select	ENSP00000338004.3:n.*140G=
ENST00000329563.8:c.*140G=	ENSP00000328973.4:n.*140G=
ENST00000337554.7:c.*140G=	ENSP00000338004.3:n.*140G=
ENST00000396265.4:c.*140G=	ENSP00000379563.4:n.*140G=
ENST00000583777.5:c.*140G=	ENSP00000463495.1:n.*140G=
NM_000714.5:c.*140G=	NP_000705.2:n.*140G=
NM_001256530.1:c.*140G=	NP_001243459.1:n.*140G=
NM_001256531.1:c.*140G=	NP_001243460.1:n.*140G=
NR_046308.1:n.559G=
NM_000714.6:c.*140G= MANE Select	NP_000705.2:n.*140G=
NR_046308.2:n.514G=