Canonical Allele Identifier: CA2738251664

Gene: TSPO

Linked Data

• dbSNP Id: rs2147060821

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43163241_43163242insTAAAAAA , CM000684.2:g.43163241_43163242insTAAAAAA	GRCh38
NC_000022.10:g.43559247_43559248insTAAAAAA , CM000684.1:g.43559247_43559248insTAAAAAA	GRCh37
NC_000022.9:g.41889191_41889192insTAAAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337554.8:c.*250_*251insTAAAAAA MANE Select	ENSP00000338004.3:n.*250_*251insTAAAAAA
ENST00000337554.7:c.*250_*251insTAAAAAA	ENSP00000338004.3:n.*250_*251insTAAAAAA
NM_000714.5:c.*250_*251insTAAAAAA	NP_000705.2:n.*250_*251insTAAAAAA
NM_001256530.1:c.*250_*251insTAAAAAA	NP_001243459.1:n.*250_*251insTAAAAAA
NM_001256531.1:c.*250_*251insTAAAAAA	NP_001243460.1:n.*250_*251insTAAAAAA
NR_046308.1:n.669_670insTAAAAAA
NM_000714.6:c.*250_*251insTAAAAAA MANE Select	NP_000705.2:n.*250_*251insTAAAAAA
NR_046308.2:n.624_625insTAAAAAA