Canonical Allele Identifier: CA2057658320
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98516038C= , CM000674.2:g.98516038C= GRCh38
NC_000012.11:g.98909816C= , CM000674.1:g.98909816C= GRCh37
NC_000012.10:g.97433947C= NCBI36
NG_021393.1:g.5466C= , LRG_443:g.5466C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556029.6:c.171C= (TMPO) MANE Select ENSP00000450627.1:p.Thr57=
ENST00000261210.9:c.171C= (TMPO) ENSP00000261210.5:p.Thr57=
ENST00000266732.8:c.171C= (TMPO) ENSP00000266732.4:p.Thr57=
ENST00000343315.9:c.171C= (TMPO) ENSP00000340251.5:p.Thr57=
ENST00000393053.6:c.171C= (TMPO) ENSP00000376773.2:p.Thr57=
ENST00000546828.6:n.229C= (TMPO)
ENST00000548911.1:n.304C= (TMPO)
ENST00000556029.5:c.171C= (TMPO) ENSP00000450627.1:p.Thr57=
NM_001032283.2:c.171C= , LRG_443t1:c.171C= (TMPO) NP_001027454.1:p.Thr57=
NM_001032284.2:c.171C= (TMPO) NP_001027455.1:p.Thr57=
NM_001307975.1:c.171C= (TMPO) NP_001294904.1:p.Thr57=
NM_003276.2:c.171C= , LRG_443t2:c.171C= (TMPO) NP_003267.1:p.Thr57=
NR_027157.1:n.189G= (TMPO-AS1)
XM_005269132.2:c.171C= (TMPO) XP_005269189.1:p.Thr57=
XM_005269132.4:c.171C= (TMPO) XP_005269189.1:p.Thr57=
NM_001032283.3:c.171C= (TMPO) MANE Select NP_001027454.1:p.Thr57=
NM_001032284.3:c.171C= (TMPO) NP_001027455.1:p.Thr57=
NM_001307975.2:c.171C= (TMPO) NP_001294904.1:p.Thr57=