Canonical Allele Identifier: CA2057658025
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98515821G= , CM000674.2:g.98515821G= GRCh38
NC_000012.11:g.98909599G= , CM000674.1:g.98909599G= GRCh37
NC_000012.10:g.97433730G= NCBI36
NG_021393.1:g.5249G= , LRG_443:g.5249G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556029.6:c.-47G= (TMPO) MANE Select ENSP00000450627.1:n.-47G=
ENST00000266732.8:c.-47G= (TMPO) ENSP00000266732.4:n.-47G=
ENST00000343315.9:c.-47G= (TMPO) ENSP00000340251.5:n.-47G=
ENST00000393053.6:c.-47G= (TMPO) ENSP00000376773.2:n.-47G=
ENST00000546828.6:n.154+36G= (TMPO)
ENST00000548911.1:n.236+7G= (TMPO)
ENST00000556029.5:c.-47G= (TMPO) ENSP00000450627.1:n.-47G=
NM_001032283.2:c.-47G= , LRG_443t1:c.-47G= (TMPO) NP_001027454.1:n.-47G=
NM_001032284.2:c.-47G= (TMPO) NP_001027455.1:n.-47G=
NM_001307975.1:c.-47G= (TMPO) NP_001294904.1:n.-47G=
NM_003276.2:c.-47G= , LRG_443t2:c.-47G= (TMPO) NP_003267.1:n.-47G=
NR_027157.1:n.313C= (TMPO-AS1)
XM_005269132.2:c.-47G= (TMPO) XP_005269189.1:n.-47G=
XM_005269132.4:c.-47G= (TMPO) XP_005269189.1:n.-47G=
NM_001032283.3:c.-47G= (TMPO) MANE Select NP_001027454.1:n.-47G=
NM_001032284.3:c.-47G= (TMPO) NP_001027455.1:n.-47G=
NM_001307975.2:c.-47G= (TMPO) NP_001294904.1:n.-47G=