Canonical Allele Identifier: CA386151059

Gene: TMPO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98531716A>G , CM000674.2:g.98531716A>G	GRCh38
NC_000012.11:g.98925494A>G , CM000674.1:g.98925494A>G	GRCh37
NC_000012.10:g.97449625A>G	NCBI36
NG_021393.1:g.21144A>G , LRG_443:g.21144A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001032283.3:c.443A>G MANE Select	NP_001027454.1:p.Lys148Arg
ENST00000556029.6:c.443A>G MANE Select	ENSP00000450627.1:p.Lys148Arg
NM_001032283.2:c.443A>G , LRG_443t1:c.443A>G	NP_001027454.1:p.Lys148Arg
NM_001032284.2:c.443A>G	NP_001027455.1:p.Lys148Arg
NM_001032284.3:c.443A>G	NP_001027455.1:p.Lys148Arg
NM_001307975.1:c.443A>G	NP_001294904.1:p.Lys148Arg
NM_001307975.2:c.443A>G	NP_001294904.1:p.Lys148Arg
NM_003276.2:c.443A>G , LRG_443t2:c.443A>G	NP_003267.1:p.Lys148Arg
ENST00000261210.9:c.443A>G	ENSP00000261210.5:p.Lys148Arg
ENST00000266732.8:c.443A>G	ENSP00000266732.4:p.Lys148Arg
ENST00000343315.9:c.443A>G	ENSP00000340251.5:p.Lys148Arg
ENST00000393053.6:c.443A>G	ENSP00000376773.2:p.Lys148Arg
ENST00000546828.6:n.501A>G
ENST00000547214.1:n.165A>G
ENST00000549938.5:n.430A>G
ENST00000552831.1:n.521A>G
ENST00000556029.5:c.443A>G	ENSP00000450627.1:p.Lys148Arg
ENST00000556678.1:c.164A>G	ENSP00000451552.1:p.Lys55Arg
XM_005269132.2:c.443A>G	XP_005269189.1:p.Lys148Arg
XM_005269132.4:c.443A>G	XP_005269189.1:p.Lys148Arg
XM_017019914.2:c.-464A>G	XP_016875403.1:n.-464A>G