Canonical Allele Identifier: CA134822

Gene: TMPO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98528002T>A , CM000674.2:g.98528002T>A	GRCh38
NC_000012.11:g.98921780T>A , CM000674.1:g.98921780T>A	GRCh37
NC_000012.10:g.97445911T>A	NCBI36
NG_021393.1:g.17430T>A , LRG_443:g.17430T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.396T>A MANE Select	ENSP00000450627.1:p.Gly132=
ENST00000261210.9:c.396T>A	ENSP00000261210.5:p.Gly132=
ENST00000266732.8:c.396T>A	ENSP00000266732.4:p.Gly132=
ENST00000343315.9:c.396T>A	ENSP00000340251.5:p.Gly132=
ENST00000393053.6:c.396T>A	ENSP00000376773.2:p.Gly132=
ENST00000546828.6:n.454T>A
ENST00000547214.1:n.118T>A
ENST00000548911.1:n.529T>A
ENST00000549938.5:n.383T>A
ENST00000552831.1:n.474T>A
ENST00000556029.5:c.396T>A	ENSP00000450627.1:p.Gly132=
ENST00000556678.1:c.117T>A	ENSP00000451552.1:p.Gly39=
NM_001032283.2:c.396T>A , LRG_443t1:c.396T>A	NP_001027454.1:p.Gly132=
NM_001032284.2:c.396T>A	NP_001027455.1:p.Gly132=
NM_001307975.1:c.396T>A	NP_001294904.1:p.Gly132=
NM_003276.2:c.396T>A , LRG_443t2:c.396T>A	NP_003267.1:p.Gly132=
XM_005269132.2:c.396T>A	XP_005269189.1:p.Gly132=
XM_005269132.4:c.396T>A	XP_005269189.1:p.Gly132=
XM_017019914.2:c.-511T>A	XP_016875403.1:n.-511T>A
NM_001032283.3:c.396T>A MANE Select	NP_001027454.1:p.Gly132=
NM_001032284.3:c.396T>A	NP_001027455.1:p.Gly132=
NM_001307975.2:c.396T>A	NP_001294904.1:p.Gly132=