Canonical Allele Identifier: CA2657109528

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162776-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162776C>A , CM000684.2:g.43162776C>A	GRCh38
NC_000022.10:g.43558782C>A , CM000684.1:g.43558782C>A	GRCh37
NC_000022.9:g.41888726C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.322-27C>A MANE Select	ENSP00000338004.3:n.322-27C>A
ENST00000329563.8:c.322-27C>A	ENSP00000328973.4:n.322-27C>A
ENST00000337554.7:c.322-27C>A	ENSP00000338004.3:n.322-27C>A
ENST00000396265.4:c.322-27C>A	ENSP00000379563.4:n.322-27C>A
ENST00000583777.5:c.10-27C>A	ENSP00000463495.1:n.10-27C>A
NM_000714.5:c.322-27C>A	NP_000705.2:n.322-27C>A
NM_001256530.1:c.322-27C>A	NP_001243459.1:n.322-27C>A
NM_001256531.1:c.322-27C>A	NP_001243460.1:n.322-27C>A
NR_046308.1:n.231-27C>A
NM_000714.6:c.322-27C>A MANE Select	NP_000705.2:n.322-27C>A
NR_046308.2:n.186-27C>A