Canonical Allele Identifier: CA2407104185

Gene: TSPO

Linked Data

• dbSNP Id: rs1931504580

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163034_43163056del , CM000684.2:g.43163034_43163056del	GRCh38
NC_000022.10:g.43559040_43559062del , CM000684.1:g.43559040_43559062del	GRCh37
NC_000022.9:g.41888984_41889006del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*43_*65del MANE Select	ENSP00000338004.3:n.*43_*65del
ENST00000329563.8:c.*43_*65del	ENSP00000328973.4:n.*43_*65del
ENST00000337554.7:c.*43_*65del	ENSP00000338004.3:n.*43_*65del
ENST00000396265.4:c.*43_*65del	ENSP00000379563.4:n.*43_*65del
ENST00000583777.5:c.*43_*65del	ENSP00000463495.1:n.*43_*65del
NM_000714.5:c.*43_*65del	NP_000705.2:n.*43_*65del
NM_001256530.1:c.*43_*65del	NP_001243459.1:n.*43_*65del
NM_001256531.1:c.*43_*65del	NP_001243460.1:n.*43_*65del
NR_046308.1:n.462_484del
NM_000714.6:c.*43_*65del MANE Select	NP_000705.2:n.*43_*65del
NR_046308.2:n.417_439del