Canonical Allele Identifier: CA481589003
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.98909549C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98515771C>A , CM000674.2:g.98515771C>A GRCh38
NC_000012.11:g.98909549C>A , CM000674.1:g.98909549C>A GRCh37
NC_000012.10:g.97433680C>A NCBI36
NG_021393.1:g.5199C>A , LRG_443:g.5199C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000556029.6:c.-97C>A (TMPO) MANE Select ENSP00000450627.1:n.-97C>A
ENST00000266732.8:c.-97C>A (TMPO) ENSP00000266732.4:n.-97C>A
ENST00000343315.9:c.-97C>A (TMPO) ENSP00000340251.5:n.-97C>A
ENST00000393053.6:c.-97C>A (TMPO) ENSP00000376773.2:n.-97C>A
ENST00000546828.6:n.140C>A (TMPO)
ENST00000548911.1:n.193C>A (TMPO)
ENST00000556029.5:c.-97C>A (TMPO) ENSP00000450627.1:n.-97C>A
NM_001032283.2:c.-97C>A , LRG_443t1:c.-97C>A (TMPO) NP_001027454.1:n.-97C>A
NM_001032284.2:c.-97C>A (TMPO) NP_001027455.1:n.-97C>A
NM_001307975.1:c.-97C>A (TMPO) NP_001294904.1:n.-97C>A
NM_003276.2:c.-97C>A , LRG_443t2:c.-97C>A (TMPO) NP_003267.1:n.-97C>A
NR_027157.1:n.363G>T (TMPO-AS1)
XM_005269132.2:c.-97C>A (TMPO) XP_005269189.1:n.-97C>A
XM_005269132.4:c.-97C>A (TMPO) XP_005269189.1:n.-97C>A
NM_001032283.3:c.-97C>A (TMPO) MANE Select NP_001027454.1:n.-97C>A
NM_001032284.3:c.-97C>A (TMPO) NP_001027455.1:n.-97C>A
NM_001307975.2:c.-97C>A (TMPO) NP_001294904.1:n.-97C>A