Canonical Allele Identifier: CA346707
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180547
dbSNP Id: rs730880228

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98516115C>T , CM000674.2:g.98516115C>T GRCh38
NC_000012.11:g.98909893C>T , CM000674.1:g.98909893C>T GRCh37
NC_000012.10:g.97434024C>T NCBI36
NG_021393.1:g.5543C>T , LRG_443:g.5543C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000556029.6:c.248C>T (TMPO) MANE Select ENSP00000450627.1:p.Ala83Val
ENST00000261210.9:c.248C>T (TMPO) ENSP00000261210.5:p.Ala83Val
ENST00000266732.8:c.248C>T (TMPO) ENSP00000266732.4:p.Ala83Val
ENST00000343315.9:c.248C>T (TMPO) ENSP00000340251.5:p.Ala83Val
ENST00000393053.6:c.248C>T (TMPO) ENSP00000376773.2:p.Ala83Val
ENST00000546828.6:n.306C>T (TMPO)
ENST00000548911.1:n.381C>T (TMPO)
ENST00000556029.5:c.248C>T (TMPO) ENSP00000450627.1:p.Ala83Val
NM_001032283.2:c.248C>T , LRG_443t1:c.248C>T (TMPO) NP_001027454.1:p.Ala83Val
NM_001032284.2:c.248C>T (TMPO) NP_001027455.1:p.Ala83Val
NM_001307975.1:c.248C>T (TMPO) NP_001294904.1:p.Ala83Val
NM_003276.2:c.248C>T , LRG_443t2:c.248C>T (TMPO) NP_003267.1:p.Ala83Val
NR_027157.1:n.112G>A (TMPO-AS1)
XM_005269132.2:c.248C>T (TMPO) XP_005269189.1:p.Ala83Val
XM_005269132.4:c.248C>T (TMPO) XP_005269189.1:p.Ala83Val
NM_001032283.3:c.248C>T (TMPO) MANE Select NP_001027454.1:p.Ala83Val
NM_001032284.3:c.248C>T (TMPO) NP_001027455.1:p.Ala83Val
NM_001307975.2:c.248C>T (TMPO) NP_001294904.1:p.Ala83Val