Canonical Allele Identifier: CA386239242

Gene: TMPO TMPO-AS1

Linked Data

• MyVariant Identifiers: chr12:g.98909655T>A (hg19) ; chr12:g.98515877T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98515877T>A , CM000674.2:g.98515877T>A	GRCh38
NC_000012.11:g.98909655T>A , CM000674.1:g.98909655T>A	GRCh37
NC_000012.10:g.97433786T>A	NCBI36
NG_021393.1:g.5305T>A , LRG_443:g.5305T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.10T>A (TMPO) MANE Select	ENSP00000450627.1:p.Phe4Ile
ENST00000261210.9:c.10T>A (TMPO)	ENSP00000261210.5:p.Phe4Ile
ENST00000266732.8:c.10T>A (TMPO)	ENSP00000266732.4:p.Phe4Ile
ENST00000343315.9:c.10T>A (TMPO)	ENSP00000340251.5:p.Phe4Ile
ENST00000393053.6:c.10T>A (TMPO)	ENSP00000376773.2:p.Phe4Ile
ENST00000546828.6:n.155-87T>A (TMPO)
ENST00000548911.1:n.236+63T>A (TMPO)
ENST00000556029.5:c.10T>A (TMPO)	ENSP00000450627.1:p.Phe4Ile
NM_001032283.2:c.10T>A , LRG_443t1:c.10T>A (TMPO)	NP_001027454.1:p.Phe4Ile
NM_001032284.2:c.10T>A (TMPO)	NP_001027455.1:p.Phe4Ile
NM_001307975.1:c.10T>A (TMPO)	NP_001294904.1:p.Phe4Ile
NM_003276.2:c.10T>A , LRG_443t2:c.10T>A (TMPO)	NP_003267.1:p.Phe4Ile
NR_027157.1:n.257A>T (TMPO-AS1)
XM_005269132.2:c.10T>A (TMPO)	XP_005269189.1:p.Phe4Ile
XM_005269132.4:c.10T>A (TMPO)	XP_005269189.1:p.Phe4Ile
NM_001032283.3:c.10T>A (TMPO) MANE Select	NP_001027454.1:p.Phe4Ile
NM_001032284.3:c.10T>A (TMPO)	NP_001027455.1:p.Phe4Ile
NM_001307975.2:c.10T>A (TMPO)	NP_001294904.1:p.Phe4Ile