Canonical Allele Identifier: CA386239793

Gene: TMPO TMPO-AS1

Linked Data

• ClinVar Variation Id: 536977
• ClinVar RCV Id: RCV000645709
• dbSNP Id: rs1555201635
• gnomAD v4: 12-98516145-G-A
• MyVariant Identifiers: chr12:g.98909923G>A (hg19) ; chr12:g.98516145G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98516145G>A , CM000674.2:g.98516145G>A	GRCh38
NC_000012.11:g.98909923G>A , CM000674.1:g.98909923G>A	GRCh37
NC_000012.10:g.97434054G>A	NCBI36
NG_021393.1:g.5573G>A , LRG_443:g.5573G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.278G>A (TMPO) MANE Select	ENSP00000450627.1:p.Arg93Lys
ENST00000261210.9:c.278G>A (TMPO)	ENSP00000261210.5:p.Arg93Lys
ENST00000266732.8:c.278G>A (TMPO)	ENSP00000266732.4:p.Arg93Lys
ENST00000343315.9:c.278G>A (TMPO)	ENSP00000340251.5:p.Arg93Lys
ENST00000393053.6:c.278G>A (TMPO)	ENSP00000376773.2:p.Arg93Lys
ENST00000546828.6:n.336G>A (TMPO)
ENST00000548911.1:n.411G>A (TMPO)
ENST00000556029.5:c.278G>A (TMPO)	ENSP00000450627.1:p.Arg93Lys
NM_001032283.2:c.278G>A , LRG_443t1:c.278G>A (TMPO)	NP_001027454.1:p.Arg93Lys
NM_001032284.2:c.278G>A (TMPO)	NP_001027455.1:p.Arg93Lys
NM_001307975.1:c.278G>A (TMPO)	NP_001294904.1:p.Arg93Lys
NM_003276.2:c.278G>A , LRG_443t2:c.278G>A (TMPO)	NP_003267.1:p.Arg93Lys
NR_027157.1:n.82C>T (TMPO-AS1)
XM_005269132.2:c.278G>A (TMPO)	XP_005269189.1:p.Arg93Lys
XM_005269132.4:c.278G>A (TMPO)	XP_005269189.1:p.Arg93Lys
NM_001032283.3:c.278G>A (TMPO) MANE Select	NP_001027454.1:p.Arg93Lys
NM_001032284.3:c.278G>A (TMPO)	NP_001027455.1:p.Arg93Lys
NM_001307975.2:c.278G>A (TMPO)	NP_001294904.1:p.Arg93Lys