Canonical Allele Identifier: CA481589872

Gene: TMPO TMPO-AS1

Linked Data

• ClinVar Variation Id: 1935483
• ClinVar RCV Id: RCV002639020
• gnomAD v4: 12-98515930-C-A
• MyVariant Identifiers: chr12:g.98909708C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98515930C>A , CM000674.2:g.98515930C>A	GRCh38
NC_000012.11:g.98909708C>A , CM000674.1:g.98909708C>A	GRCh37
NC_000012.10:g.97433839C>A	NCBI36
NG_021393.1:g.5358C>A , LRG_443:g.5358C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.63C>A (TMPO) MANE Select	ENSP00000450627.1:p.Val21=
ENST00000261210.9:c.63C>A (TMPO)	ENSP00000261210.5:p.Val21=
ENST00000266732.8:c.63C>A (TMPO)	ENSP00000266732.4:p.Val21=
ENST00000343315.9:c.63C>A (TMPO)	ENSP00000340251.5:p.Val21=
ENST00000393053.6:c.63C>A (TMPO)	ENSP00000376773.2:p.Val21=
ENST00000546828.6:n.155-34C>A (TMPO)
ENST00000548911.1:n.237-41C>A (TMPO)
ENST00000556029.5:c.63C>A (TMPO)	ENSP00000450627.1:p.Val21=
NM_001032283.2:c.63C>A , LRG_443t1:c.63C>A (TMPO)	NP_001027454.1:p.Val21=
NM_001032284.2:c.63C>A (TMPO)	NP_001027455.1:p.Val21=
NM_001307975.1:c.63C>A (TMPO)	NP_001294904.1:p.Val21=
NM_003276.2:c.63C>A , LRG_443t2:c.63C>A (TMPO)	NP_003267.1:p.Val21=
NR_027157.1:n.237-33G>T (TMPO-AS1)
XM_005269132.2:c.63C>A (TMPO)	XP_005269189.1:p.Val21=
XM_005269132.4:c.63C>A (TMPO)	XP_005269189.1:p.Val21=
NM_001032283.3:c.63C>A (TMPO) MANE Select	NP_001027454.1:p.Val21=
NM_001032284.3:c.63C>A (TMPO)	NP_001027455.1:p.Val21=
NM_001307975.2:c.63C>A (TMPO)	NP_001294904.1:p.Val21=