Canonical Allele Identifier: CA386239359

Gene: TMPO TMPO-AS1

Linked Data

• MyVariant Identifiers: chr12:g.98909707T>C (hg19) ; chr12:g.98515929T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98515929T>C , CM000674.2:g.98515929T>C	GRCh38
NC_000012.11:g.98909707T>C , CM000674.1:g.98909707T>C	GRCh37
NC_000012.10:g.97433838T>C	NCBI36
NG_021393.1:g.5357T>C , LRG_443:g.5357T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.62T>C (TMPO) MANE Select	ENSP00000450627.1:p.Val21Ala
ENST00000261210.9:c.62T>C (TMPO)	ENSP00000261210.5:p.Val21Ala
ENST00000266732.8:c.62T>C (TMPO)	ENSP00000266732.4:p.Val21Ala
ENST00000343315.9:c.62T>C (TMPO)	ENSP00000340251.5:p.Val21Ala
ENST00000393053.6:c.62T>C (TMPO)	ENSP00000376773.2:p.Val21Ala
ENST00000546828.6:n.155-35T>C (TMPO)
ENST00000548911.1:n.237-42T>C (TMPO)
ENST00000556029.5:c.62T>C (TMPO)	ENSP00000450627.1:p.Val21Ala
NM_001032283.2:c.62T>C , LRG_443t1:c.62T>C (TMPO)	NP_001027454.1:p.Val21Ala
NM_001032284.2:c.62T>C (TMPO)	NP_001027455.1:p.Val21Ala
NM_001307975.1:c.62T>C (TMPO)	NP_001294904.1:p.Val21Ala
NM_003276.2:c.62T>C , LRG_443t2:c.62T>C (TMPO)	NP_003267.1:p.Val21Ala
NR_027157.1:n.237-32A>G (TMPO-AS1)
XM_005269132.2:c.62T>C (TMPO)	XP_005269189.1:p.Val21Ala
XM_005269132.4:c.62T>C (TMPO)	XP_005269189.1:p.Val21Ala
NM_001032283.3:c.62T>C (TMPO) MANE Select	NP_001027454.1:p.Val21Ala
NM_001032284.3:c.62T>C (TMPO)	NP_001027455.1:p.Val21Ala
NM_001307975.2:c.62T>C (TMPO)	NP_001294904.1:p.Val21Ala