Canonical Allele Identifier: CA2057658492
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98516150A= , CM000674.2:g.98516150A= GRCh38
NC_000012.11:g.98909928A= , CM000674.1:g.98909928A= GRCh37
NC_000012.10:g.97434059A= NCBI36
NG_021393.1:g.5578A= , LRG_443:g.5578A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556029.6:c.279+4A= (TMPO) MANE Select ENSP00000450627.1:n.279+4A=
ENST00000261210.9:c.279+4A= (TMPO) ENSP00000261210.5:n.279+4A=
ENST00000266732.8:c.279+4A= (TMPO) ENSP00000266732.4:n.279+4A=
ENST00000343315.9:c.279+4A= (TMPO) ENSP00000340251.5:n.279+4A=
ENST00000393053.6:c.279+4A= (TMPO) ENSP00000376773.2:n.279+4A=
ENST00000546828.6:n.337+4A= (TMPO)
ENST00000548911.1:n.412+4A= (TMPO)
ENST00000556029.5:c.279+4A= (TMPO) ENSP00000450627.1:n.279+4A=
NM_001032283.2:c.279+4A= , LRG_443t1:c.279+4A= (TMPO) NP_001027454.1:n.279+4A=
NM_001032284.2:c.279+4A= (TMPO) NP_001027455.1:n.279+4A=
NM_001307975.1:c.279+4A= (TMPO) NP_001294904.1:n.279+4A=
NM_003276.2:c.279+4A= , LRG_443t2:c.279+4A= (TMPO) NP_003267.1:n.279+4A=
NR_027157.1:n.77T= (TMPO-AS1)
XM_005269132.2:c.279+4A= (TMPO) XP_005269189.1:n.279+4A=
XM_005269132.4:c.279+4A= (TMPO) XP_005269189.1:n.279+4A=
NM_001032283.3:c.279+4A= (TMPO) MANE Select NP_001027454.1:n.279+4A=
NM_001032284.3:c.279+4A= (TMPO) NP_001027455.1:n.279+4A=
NM_001307975.2:c.279+4A= (TMPO) NP_001294904.1:n.279+4A=