Canonical Allele Identifier: CA6732079

Gene: TMPO TMPO-AS1

Linked Data

• dbSNP Id: rs755207935
• ExAC: 12:98909599 G / C
• gnomAD v2: 12-98909599-G-C
• gnomAD v3: 12-98515821-G-C
• gnomAD v4: 12-98515821-G-C
• MyVariant Identifiers: chr12:g.98909599G>C (hg19) ; chr12:g.98515821G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98515821G>C , CM000674.2:g.98515821G>C	GRCh38
NC_000012.11:g.98909599G>C , CM000674.1:g.98909599G>C	GRCh37
NC_000012.10:g.97433730G>C	NCBI36
NG_021393.1:g.5249G>C , LRG_443:g.5249G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.-47G>C (TMPO) MANE Select	ENSP00000450627.1:n.-47G>C
ENST00000266732.8:c.-47G>C (TMPO)	ENSP00000266732.4:n.-47G>C
ENST00000343315.9:c.-47G>C (TMPO)	ENSP00000340251.5:n.-47G>C
ENST00000393053.6:c.-47G>C (TMPO)	ENSP00000376773.2:n.-47G>C
ENST00000546828.6:n.154+36G>C (TMPO)
ENST00000548911.1:n.236+7G>C (TMPO)
ENST00000556029.5:c.-47G>C (TMPO)	ENSP00000450627.1:n.-47G>C
NM_001032283.2:c.-47G>C , LRG_443t1:c.-47G>C (TMPO)	NP_001027454.1:n.-47G>C
NM_001032284.2:c.-47G>C (TMPO)	NP_001027455.1:n.-47G>C
NM_001307975.1:c.-47G>C (TMPO)	NP_001294904.1:n.-47G>C
NM_003276.2:c.-47G>C , LRG_443t2:c.-47G>C (TMPO)	NP_003267.1:n.-47G>C
NR_027157.1:n.313C>G (TMPO-AS1)
XM_005269132.2:c.-47G>C (TMPO)	XP_005269189.1:n.-47G>C
XM_005269132.4:c.-47G>C (TMPO)	XP_005269189.1:n.-47G>C
NM_001032283.3:c.-47G>C (TMPO) MANE Select	NP_001027454.1:n.-47G>C
NM_001032284.3:c.-47G>C (TMPO)	NP_001027455.1:n.-47G>C
NM_001307975.2:c.-47G>C (TMPO)	NP_001294904.1:n.-47G>C