Canonical Allele Identifier: CA2657109613

Gene: TSPO

Linked Data

• gnomAD v4: 22-43163035-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163035T>C , CM000684.2:g.43163035T>C	GRCh38
NC_000022.10:g.43559041T>C , CM000684.1:g.43559041T>C	GRCh37
NC_000022.9:g.41888985T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*44T>C MANE Select	ENSP00000338004.3:n.*44T>C
ENST00000329563.8:c.*44T>C	ENSP00000328973.4:n.*44T>C
ENST00000337554.7:c.*44T>C	ENSP00000338004.3:n.*44T>C
ENST00000396265.4:c.*44T>C	ENSP00000379563.4:n.*44T>C
ENST00000583777.5:c.*44T>C	ENSP00000463495.1:n.*44T>C
NM_000714.5:c.*44T>C	NP_000705.2:n.*44T>C
NM_001256530.1:c.*44T>C	NP_001243459.1:n.*44T>C
NM_001256531.1:c.*44T>C	NP_001243460.1:n.*44T>C
NR_046308.1:n.463T>C
NM_000714.6:c.*44T>C MANE Select	NP_000705.2:n.*44T>C
NR_046308.2:n.418T>C