Canonical Allele Identifier: CA324776102

Gene: TSPO

Linked Data

• dbSNP Id: rs377258040
• gnomAD v3: 22-43163078-G-C
• gnomAD v4: 22-43163078-G-C
• MyVariant Identifiers: chr22:g.43559084G>C (hg19) ; chr22:g.43163078G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163078G>C , CM000684.2:g.43163078G>C	GRCh38
NC_000022.10:g.43559084G>C , CM000684.1:g.43559084G>C	GRCh37
NC_000022.9:g.41889028G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*87G>C MANE Select	ENSP00000338004.3:n.*87G>C
ENST00000329563.8:c.*87G>C	ENSP00000328973.4:n.*87G>C
ENST00000337554.7:c.*87G>C	ENSP00000338004.3:n.*87G>C
ENST00000396265.4:c.*87G>C	ENSP00000379563.4:n.*87G>C
ENST00000583777.5:c.*87G>C	ENSP00000463495.1:n.*87G>C
NM_000714.5:c.*87G>C	NP_000705.2:n.*87G>C
NM_001256530.1:c.*87G>C	NP_001243459.1:n.*87G>C
NM_001256531.1:c.*87G>C	NP_001243460.1:n.*87G>C
NR_046308.1:n.506G>C
NM_000714.6:c.*87G>C MANE Select	NP_000705.2:n.*87G>C
NR_046308.2:n.461G>C