Canonical Allele Identifier: CA10587755
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 263441
ClinVar RCV Id: RCV000252187
dbSNP Id: rs886038806

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98515891C>T , CM000674.2:g.98515891C>T GRCh38
NC_000012.11:g.98909669C>T , CM000674.1:g.98909669C>T GRCh37
NC_000012.10:g.97433800C>T NCBI36
NG_021393.1:g.5319C>T , LRG_443:g.5319C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000556029.6:c.24C>T (TMPO) MANE Select ENSP00000450627.1:p.Pro8=
ENST00000261210.9:c.24C>T (TMPO) ENSP00000261210.5:p.Pro8=
ENST00000266732.8:c.24C>T (TMPO) ENSP00000266732.4:p.Pro8=
ENST00000343315.9:c.24C>T (TMPO) ENSP00000340251.5:p.Pro8=
ENST00000393053.6:c.24C>T (TMPO) ENSP00000376773.2:p.Pro8=
ENST00000546828.6:n.155-73C>T (TMPO)
ENST00000548911.1:n.236+77C>T (TMPO)
ENST00000556029.5:c.24C>T (TMPO) ENSP00000450627.1:p.Pro8=
NM_001032283.2:c.24C>T , LRG_443t1:c.24C>T (TMPO) NP_001027454.1:p.Pro8=
NM_001032284.2:c.24C>T (TMPO) NP_001027455.1:p.Pro8=
NM_001307975.1:c.24C>T (TMPO) NP_001294904.1:p.Pro8=
NM_003276.2:c.24C>T , LRG_443t2:c.24C>T (TMPO) NP_003267.1:p.Pro8=
NR_027157.1:n.243G>A (TMPO-AS1)
XM_005269132.2:c.24C>T (TMPO) XP_005269189.1:p.Pro8=
XM_005269132.4:c.24C>T (TMPO) XP_005269189.1:p.Pro8=
NM_001032283.3:c.24C>T (TMPO) MANE Select NP_001027454.1:p.Pro8=
NM_001032284.3:c.24C>T (TMPO) NP_001027455.1:p.Pro8=
NM_001307975.2:c.24C>T (TMPO) NP_001294904.1:p.Pro8=