Canonical Allele Identifier: CA481589427
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.98909607G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98515829G>T , CM000674.2:g.98515829G>T GRCh38
NC_000012.11:g.98909607G>T , CM000674.1:g.98909607G>T GRCh37
NC_000012.10:g.97433738G>T NCBI36
NG_021393.1:g.5257G>T , LRG_443:g.5257G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000556029.6:c.-39G>T (TMPO) MANE Select ENSP00000450627.1:n.-39G>T
ENST00000266732.8:c.-39G>T (TMPO) ENSP00000266732.4:n.-39G>T
ENST00000343315.9:c.-39G>T (TMPO) ENSP00000340251.5:n.-39G>T
ENST00000393053.6:c.-39G>T (TMPO) ENSP00000376773.2:n.-39G>T
ENST00000546828.6:n.154+44G>T (TMPO)
ENST00000548911.1:n.236+15G>T (TMPO)
ENST00000556029.5:c.-39G>T (TMPO) ENSP00000450627.1:n.-39G>T
NM_001032283.2:c.-39G>T , LRG_443t1:c.-39G>T (TMPO) NP_001027454.1:n.-39G>T
NM_001032284.2:c.-39G>T (TMPO) NP_001027455.1:n.-39G>T
NM_001307975.1:c.-39G>T (TMPO) NP_001294904.1:n.-39G>T
NM_003276.2:c.-39G>T , LRG_443t2:c.-39G>T (TMPO) NP_003267.1:n.-39G>T
NR_027157.1:n.305C>A (TMPO-AS1)
XM_005269132.2:c.-39G>T (TMPO) XP_005269189.1:n.-39G>T
XM_005269132.4:c.-39G>T (TMPO) XP_005269189.1:n.-39G>T
NM_001032283.3:c.-39G>T (TMPO) MANE Select NP_001027454.1:n.-39G>T
NM_001032284.3:c.-39G>T (TMPO) NP_001027455.1:n.-39G>T
NM_001307975.2:c.-39G>T (TMPO) NP_001294904.1:n.-39G>T