Canonical Allele Identifier: CA481589640

Gene: TMPO TMPO-AS1

Linked Data

• ClinVar Variation Id: 1784211
• ClinVar RCV Id: RCV004059457
• dbSNP Id: rs1229477397
• gnomAD v3: 12-98515867-G-C
• gnomAD v4: 12-98515867-G-C
• MyVariant Identifiers: chr12:g.98909645G>C (hg19) ; chr12:g.98515867G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98515867G>C , CM000674.2:g.98515867G>C	GRCh38
NC_000012.11:g.98909645G>C , CM000674.1:g.98909645G>C	GRCh37
NC_000012.10:g.97433776G>C	NCBI36
NG_021393.1:g.5295G>C , LRG_443:g.5295G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.-1G>C (TMPO) MANE Select	ENSP00000450627.1:n.-1G>C
ENST00000261210.9:c.-1G>C (TMPO)	ENSP00000261210.5:n.-1G>C
ENST00000266732.8:c.-1G>C (TMPO)	ENSP00000266732.4:n.-1G>C
ENST00000343315.9:c.-1G>C (TMPO)	ENSP00000340251.5:n.-1G>C
ENST00000393053.6:c.-1G>C (TMPO)	ENSP00000376773.2:n.-1G>C
ENST00000546828.6:n.154+82G>C (TMPO)
ENST00000548911.1:n.236+53G>C (TMPO)
ENST00000556029.5:c.-1G>C (TMPO)	ENSP00000450627.1:n.-1G>C
NM_001032283.2:c.-1G>C , LRG_443t1:c.-1G>C (TMPO)	NP_001027454.1:n.-1G>C
NM_001032284.2:c.-1G>C (TMPO)	NP_001027455.1:n.-1G>C
NM_001307975.1:c.-1G>C (TMPO)	NP_001294904.1:n.-1G>C
NM_003276.2:c.-1G>C , LRG_443t2:c.-1G>C (TMPO)	NP_003267.1:n.-1G>C
NR_027157.1:n.267C>G (TMPO-AS1)
XM_005269132.2:c.-1G>C (TMPO)	XP_005269189.1:n.-1G>C
XM_005269132.4:c.-1G>C (TMPO)	XP_005269189.1:n.-1G>C
NM_001032283.3:c.-1G>C (TMPO) MANE Select	NP_001027454.1:n.-1G>C
NM_001032284.3:c.-1G>C (TMPO)	NP_001027455.1:n.-1G>C
NM_001307975.2:c.-1G>C (TMPO)	NP_001294904.1:n.-1G>C