Canonical Allele Identifier: CA386239767
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98516134_98516136del , CM000674.2:g.98516134_98516136del GRCh38
NC_000012.11:g.98909912_98909914del , CM000674.1:g.98909912_98909914del GRCh37
NC_000012.10:g.97434043_97434045del NCBI36
NG_021393.1:g.5562_5564del , LRG_443:g.5562_5564del

Transcript Alleles

HGVS Amino-acid Change
ENST00000556029.6:c.267_269del (TMPO) MANE Select ENSP00000450627.1:p.Ala90del
ENST00000261210.9:c.267_269del (TMPO) ENSP00000261210.5:p.Ala90del
ENST00000266732.8:c.267_269del (TMPO) ENSP00000266732.4:p.Ala90del
ENST00000343315.9:c.267_269del (TMPO) ENSP00000340251.5:p.Ala90del
ENST00000393053.6:c.267_269del (TMPO) ENSP00000376773.2:p.Ala90del
ENST00000546828.6:n.325_327del (TMPO)
ENST00000548911.1:n.400_402del (TMPO)
ENST00000556029.5:c.267_269del (TMPO) ENSP00000450627.1:p.Ala90del
NM_001032283.2:c.267_269del , LRG_443t1:c.267_269del (TMPO) NP_001027454.1:p.Ala90del
NM_001032284.2:c.267_269del (TMPO) NP_001027455.1:p.Ala90del
NM_001307975.1:c.267_269del (TMPO) NP_001294904.1:p.Ala90del
NM_003276.2:c.267_269del , LRG_443t2:c.267_269del (TMPO) NP_003267.1:p.Ala90del
NR_027157.1:n.94_96del (TMPO-AS1)
XM_005269132.2:c.267_269del (TMPO) XP_005269189.1:p.Ala90del
XM_005269132.4:c.267_269del (TMPO) XP_005269189.1:p.Ala90del
NM_001032283.3:c.267_269del (TMPO) MANE Select NP_001027454.1:p.Ala90del
NM_001032284.3:c.267_269del (TMPO) NP_001027455.1:p.Ala90del
NM_001307975.2:c.267_269del (TMPO) NP_001294904.1:p.Ala90del