Canonical Allele Identifier: CA2657109557

Gene: TSPO

Linked Data

• gnomAD v4: 22-43162869-AGCCCGCTGGCCGCCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162873_43162887del , CM000684.2:g.43162873_43162887del	GRCh38
NC_000022.10:g.43558879_43558893del , CM000684.1:g.43558879_43558893del	GRCh37
NC_000022.9:g.41888823_41888837del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.392_406del MANE Select	ENSP00000338004.3:p.Pro131_Arg135del
ENST00000329563.8:c.392_406del	ENSP00000328973.4:p.Pro131_Arg135del
ENST00000337554.7:c.392_406del	ENSP00000338004.3:p.Pro131_Arg135del
ENST00000396265.4:c.392_406del	ENSP00000379563.4:p.Pro131_Arg135del
ENST00000583777.5:c.80_94del	ENSP00000463495.1:p.Pro27_Arg31del
NM_000714.5:c.392_406del	NP_000705.2:p.Pro131_Arg135del
NM_001256530.1:c.392_406del	NP_001243459.1:p.Pro131_Arg135del
NM_001256531.1:c.392_406del	NP_001243460.1:p.Pro131_Arg135del
NR_046308.1:n.301_315del
NM_000714.6:c.392_406del MANE Select	NP_000705.2:p.Pro131_Arg135del
NR_046308.2:n.256_270del