Canonical Allele Identifier: CA514828345
Gene: TSPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.43558829G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162823G>C , CM000684.2:g.43162823G>C GRCh38
NC_000022.10:g.43558829G>C , CM000684.1:g.43558829G>C GRCh37
NC_000022.9:g.41888773G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.342G>C MANE Select ENSP00000338004.3:p.Leu114=
ENST00000329563.8:c.342G>C ENSP00000328973.4:p.Leu114=
ENST00000337554.7:c.342G>C ENSP00000338004.3:p.Leu114=
ENST00000396265.4:c.342G>C ENSP00000379563.4:p.Leu114=
ENST00000583777.5:c.30G>C ENSP00000463495.1:p.Leu10=
NM_000714.5:c.342G>C NP_000705.2:p.Leu114=
NM_001256530.1:c.342G>C NP_001243459.1:p.Leu114=
NM_001256531.1:c.342G>C NP_001243460.1:p.Leu114=
NR_046308.1:n.251G>C
NM_000714.6:c.342G>C MANE Select NP_000705.2:p.Leu114=
NR_046308.2:n.206G>C