Canonical Allele Identifier: CA6732078
Gene: TMPO HGNC NCBI
TMPO-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs769833482
ExAC: 12:98909598 A / AGCG
gnomAD v2: 12-98909598-A-AGCG
gnomAD v3: 12-98515820-A-AGCG
gnomAD v4: 12-98515820-A-AGCG
MyVariant Identifiers: chr12:g.98909607_98909608insGCG (hg19) chr12:g.98909598_98909599insGCG (hg19) chr12:g.98515820_98515821insGCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98515829_98515831dup , CM000674.2:g.98515829_98515831dup GRCh38
NC_000012.11:g.98909607_98909609dup , CM000674.1:g.98909607_98909609dup GRCh37
NC_000012.10:g.97433738_97433740dup NCBI36
NG_021393.1:g.5257_5259dup , LRG_443:g.5257_5259dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000556029.6:c.-39_-37dup (TMPO) MANE Select ENSP00000450627.1:n.-39_-37dup
ENST00000266732.8:c.-39_-37dup (TMPO) ENSP00000266732.4:n.-39_-37dup
ENST00000343315.9:c.-39_-37dup (TMPO) ENSP00000340251.5:n.-39_-37dup
ENST00000393053.6:c.-39_-37dup (TMPO) ENSP00000376773.2:n.-39_-37dup
ENST00000546828.6:n.154+44_154+46dup (TMPO)
ENST00000548911.1:n.236+15_236+17dup (TMPO)
ENST00000556029.5:c.-39_-37dup (TMPO) ENSP00000450627.1:n.-39_-37dup
NM_001032283.2:c.-39_-37dup , LRG_443t1:c.-39_-37dup (TMPO) NP_001027454.1:n.-39_-37dup
NM_001032284.2:c.-39_-37dup (TMPO) NP_001027455.1:n.-39_-37dup
NM_001307975.1:c.-39_-37dup (TMPO) NP_001294904.1:n.-39_-37dup
NM_003276.2:c.-39_-37dup , LRG_443t2:c.-39_-37dup (TMPO) NP_003267.1:n.-39_-37dup
NR_027157.1:n.311_313dup (TMPO-AS1)
XM_005269132.2:c.-39_-37dup (TMPO) XP_005269189.1:n.-39_-37dup
XM_005269132.4:c.-39_-37dup (TMPO) XP_005269189.1:n.-39_-37dup
NM_001032283.3:c.-39_-37dup (TMPO) MANE Select NP_001027454.1:n.-39_-37dup
NM_001032284.3:c.-39_-37dup (TMPO) NP_001027455.1:n.-39_-37dup
NM_001307975.2:c.-39_-37dup (TMPO) NP_001294904.1:n.-39_-37dup
Search 100 bp 5'
Search 100 bp 3'