Canonical Allele Identifier: CA411817230

Gene: TSPO

Linked Data

• MyVariant Identifiers: chr22:g.43163028del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163029del , CM000684.2:g.43163029del	GRCh38
NC_000022.10:g.43559035del , CM000684.1:g.43559035del	GRCh37
NC_000022.9:g.41888979del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*38del MANE Select	ENSP00000338004.3:n.*38del
ENST00000329563.8:c.*38del	ENSP00000328973.4:n.*38del
ENST00000337554.7:c.*38del	ENSP00000338004.3:n.*38del
ENST00000396265.4:c.*38del	ENSP00000379563.4:n.*38del
ENST00000583777.5:c.*38del	ENSP00000463495.1:n.*38del
NM_000714.5:c.*38del	NP_000705.2:n.*38del
NM_001256530.1:c.*38del	NP_001243459.1:n.*38del
NM_001256531.1:c.*38del	NP_001243460.1:n.*38del
NR_046308.1:n.457del
NM_000714.6:c.*38del MANE Select	NP_000705.2:n.*38del
NR_046308.2:n.412del