Canonical Allele Identifier: CA242223461

Gene: TMPO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98531461C>T , CM000674.2:g.98531461C>T	GRCh38
NC_000012.11:g.98925239C>T , CM000674.1:g.98925239C>T	GRCh37
NC_000012.10:g.97449370C>T	NCBI36
NG_021393.1:g.20889C>T , LRG_443:g.20889C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001032283.3:c.407-219C>T MANE Select	NP_001027454.1:n.407-219C>T
ENST00000556029.6:c.407-219C>T MANE Select	ENSP00000450627.1:n.407-219C>T
NM_001032283.2:c.407-219C>T , LRG_443t1:c.407-219C>T	NP_001027454.1:n.407-219C>T
NM_001032284.2:c.407-219C>T	NP_001027455.1:n.407-219C>T
NM_001032284.3:c.407-219C>T	NP_001027455.1:n.407-219C>T
NM_001307975.1:c.407-219C>T	NP_001294904.1:n.407-219C>T
NM_001307975.2:c.407-219C>T	NP_001294904.1:n.407-219C>T
NM_003276.2:c.407-219C>T , LRG_443t2:c.407-219C>T	NP_003267.1:n.407-219C>T
ENST00000261210.9:c.407-219C>T	ENSP00000261210.5:n.407-219C>T
ENST00000266732.8:c.407-219C>T	ENSP00000266732.4:n.407-219C>T
ENST00000343315.9:c.407-219C>T	ENSP00000340251.5:n.407-219C>T
ENST00000393053.6:c.407-219C>T	ENSP00000376773.2:n.407-219C>T
ENST00000546828.6:n.465-219C>T
ENST00000547214.1:n.129-219C>T
ENST00000549938.5:n.394-219C>T
ENST00000552831.1:n.485-219C>T
ENST00000556029.5:c.407-219C>T	ENSP00000450627.1:n.407-219C>T
ENST00000556678.1:c.128-219C>T	ENSP00000451552.1:n.128-219C>T
XM_005269132.2:c.407-219C>T	XP_005269189.1:n.407-219C>T
XM_005269132.4:c.407-219C>T	XP_005269189.1:n.407-219C>T
XM_017019914.2:c.-500-219C>T	XP_016875403.1:n.-500-219C>T