Canonical Allele Identifier: CA6732136

Gene: TMPO TMPO-AS1

Linked Data

• ClinVar Variation Id: 416241
• ClinVar RCV Id: RCV001447383 ; RCV003352882
• dbSNP Id: rs753917997
• ExAC: 12:98909879 C / T
• gnomAD v2: 12-98909879-C-T
• gnomAD v3: 12-98516101-C-T
• gnomAD v4: 12-98516101-C-T
• MyVariant Identifiers: chr12:g.98909879C>T (hg19) ; chr12:g.98516101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98516101C>T , CM000674.2:g.98516101C>T	GRCh38
NC_000012.11:g.98909879C>T , CM000674.1:g.98909879C>T	GRCh37
NC_000012.10:g.97434010C>T	NCBI36
NG_021393.1:g.5529C>T , LRG_443:g.5529C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000556029.6:c.234C>T (TMPO) MANE Select	ENSP00000450627.1:p.Gly78=
ENST00000261210.9:c.234C>T (TMPO)	ENSP00000261210.5:p.Gly78=
ENST00000266732.8:c.234C>T (TMPO)	ENSP00000266732.4:p.Gly78=
ENST00000343315.9:c.234C>T (TMPO)	ENSP00000340251.5:p.Gly78=
ENST00000393053.6:c.234C>T (TMPO)	ENSP00000376773.2:p.Gly78=
ENST00000546828.6:n.292C>T (TMPO)
ENST00000548911.1:n.367C>T (TMPO)
ENST00000556029.5:c.234C>T (TMPO)	ENSP00000450627.1:p.Gly78=
NM_001032283.2:c.234C>T , LRG_443t1:c.234C>T (TMPO)	NP_001027454.1:p.Gly78=
NM_001032284.2:c.234C>T (TMPO)	NP_001027455.1:p.Gly78=
NM_001307975.1:c.234C>T (TMPO)	NP_001294904.1:p.Gly78=
NM_003276.2:c.234C>T , LRG_443t2:c.234C>T (TMPO)	NP_003267.1:p.Gly78=
NR_027157.1:n.126G>A (TMPO-AS1)
XM_005269132.2:c.234C>T (TMPO)	XP_005269189.1:p.Gly78=
XM_005269132.4:c.234C>T (TMPO)	XP_005269189.1:p.Gly78=
NM_001032283.3:c.234C>T (TMPO) MANE Select	NP_001027454.1:p.Gly78=
NM_001032284.3:c.234C>T (TMPO)	NP_001027455.1:p.Gly78=
NM_001307975.2:c.234C>T (TMPO)	NP_001294904.1:p.Gly78=