Canonical Allele Identifier: CA481589194

Gene: TMPO TMPO-AS1

Linked Data

• gnomAD v4: 12-98515799-A-G
• MyVariant Identifiers: chr12:g.98909577A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98515799A>G , CM000674.2:g.98515799A>G	GRCh38
NC_000012.11:g.98909577A>G , CM000674.1:g.98909577A>G	GRCh37
NC_000012.10:g.97433708A>G	NCBI36
NG_021393.1:g.5227A>G , LRG_443:g.5227A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.-69A>G (TMPO) MANE Select	ENSP00000450627.1:n.-69A>G
ENST00000266732.8:c.-69A>G (TMPO)	ENSP00000266732.4:n.-69A>G
ENST00000343315.9:c.-69A>G (TMPO)	ENSP00000340251.5:n.-69A>G
ENST00000393053.6:c.-69A>G (TMPO)	ENSP00000376773.2:n.-69A>G
ENST00000546828.6:n.154+14A>G (TMPO)
ENST00000548911.1:n.221A>G (TMPO)
ENST00000556029.5:c.-69A>G (TMPO)	ENSP00000450627.1:n.-69A>G
NM_001032283.2:c.-69A>G , LRG_443t1:c.-69A>G (TMPO)	NP_001027454.1:n.-69A>G
NM_001032284.2:c.-69A>G (TMPO)	NP_001027455.1:n.-69A>G
NM_001307975.1:c.-69A>G (TMPO)	NP_001294904.1:n.-69A>G
NM_003276.2:c.-69A>G , LRG_443t2:c.-69A>G (TMPO)	NP_003267.1:n.-69A>G
NR_027157.1:n.335T>C (TMPO-AS1)
XM_005269132.2:c.-69A>G (TMPO)	XP_005269189.1:n.-69A>G
XM_005269132.4:c.-69A>G (TMPO)	XP_005269189.1:n.-69A>G
NM_001032283.3:c.-69A>G (TMPO) MANE Select	NP_001027454.1:n.-69A>G
NM_001032284.3:c.-69A>G (TMPO)	NP_001027455.1:n.-69A>G
NM_001307975.2:c.-69A>G (TMPO)	NP_001294904.1:n.-69A>G