Canonical Allele Identifier: CA6732167

Gene: TMPO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98527924T>A , CM000674.2:g.98527924T>A	GRCh38
NC_000012.11:g.98921702T>A , CM000674.1:g.98921702T>A	GRCh37
NC_000012.10:g.97445833T>A	NCBI36
NG_021393.1:g.17352T>A , LRG_443:g.17352T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001032283.3:c.318T>A MANE Select	NP_001027454.1:p.Asp106Glu
ENST00000556029.6:c.318T>A MANE Select	ENSP00000450627.1:p.Asp106Glu
NM_001032283.2:c.318T>A , LRG_443t1:c.318T>A	NP_001027454.1:p.Asp106Glu
NM_001032284.2:c.318T>A	NP_001027455.1:p.Asp106Glu
NM_001032284.3:c.318T>A	NP_001027455.1:p.Asp106Glu
NM_001307975.1:c.318T>A	NP_001294904.1:p.Asp106Glu
NM_001307975.2:c.318T>A	NP_001294904.1:p.Asp106Glu
NM_003276.2:c.318T>A , LRG_443t2:c.318T>A	NP_003267.1:p.Asp106Glu
ENST00000261210.9:c.318T>A	ENSP00000261210.5:p.Asp106Glu
ENST00000266732.8:c.318T>A	ENSP00000266732.4:p.Asp106Glu
ENST00000343315.9:c.318T>A	ENSP00000340251.5:p.Asp106Glu
ENST00000393053.6:c.318T>A	ENSP00000376773.2:p.Asp106Glu
ENST00000546828.6:n.376T>A
ENST00000547214.1:n.40T>A
ENST00000548911.1:n.451T>A
ENST00000549938.5:n.305T>A
ENST00000552831.1:n.396T>A
ENST00000556029.5:c.318T>A	ENSP00000450627.1:p.Asp106Glu
ENST00000556678.1:c.39T>A	ENSP00000451552.1:p.Asp13Glu
XM_005269132.2:c.318T>A	XP_005269189.1:p.Asp106Glu
XM_005269132.4:c.318T>A	XP_005269189.1:p.Asp106Glu
XM_017019914.2:c.-589T>A	XP_016875403.1:n.-589T>A