Canonical Allele Identifier: CA166236998

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128957309C>T , CM000669.2:g.128957309C>T	GRCh38
NC_000007.13:g.128597363C>T , CM000669.1:g.128597363C>T	GRCh37
NC_000007.12:g.128384599C>T	NCBI36
NG_023428.1:g.102865G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012470.4:c.2718G>A MANE Select	NP_036602.1:p.Glu906=
ENST00000265388.10:c.2718G>A MANE Select	ENSP00000265388.5:p.Glu906=
NM_001191028.2:c.2526G>A	NP_001177957.2:p.Glu842=
NM_001191028.3:c.2526G>A	NP_001177957.2:p.Glu842=
NM_001382216.1:c.2820G>A	NP_001369145.1:p.Glu940=
NM_001382217.1:c.2799G>A	NP_001369146.1:p.Glu933=
NM_001382218.1:c.2712-1924G>A	NP_001369147.1:n.2712-1924G>A
NM_001382219.1:c.2610G>A	NP_001369148.1:p.Glu870=
NM_001382220.1:c.2577G>A	NP_001369149.1:p.Glu859=
NM_001382221.1:c.2574G>A	NP_001369150.1:p.Glu858=
NM_001382222.1:c.2571G>A	NP_001369151.1:p.Glu857=
NM_001382223.1:c.2520-1924G>A	NP_001369152.1:n.2520-1924G>A
NM_012470.3:c.2718G>A	NP_036602.1:p.Glu906=
NR_034053.2:n.3282G>A
NR_034053.3:n.3220G>A
NR_167911.1:n.3307G>A
NR_167912.1:n.3165G>A
NR_167913.1:n.2967G>A
NR_167914.1:n.3127G>A
NR_167915.1:n.3383G>A
NR_167916.1:n.2857G>A
NR_167917.1:n.2890G>A
NR_167918.1:n.3345G>A
NR_167919.1:n.3184G>A
NR_167920.1:n.3143G>A
NR_167921.1:n.3345G>A
NR_167922.1:n.3181G>A
NR_167923.1:n.2982G>A
NR_167924.1:n.3210G>A
NR_167925.1:n.2982G>A
NR_167926.1:n.2993G>A
NR_167927.1:n.3286G>A
ENST00000265388.9:c.2718G>A	ENSP00000265388.5:p.Glu906=
ENST00000471166.1:c.2820G>A	ENSP00000418267.1:p.Glu940=
ENST00000471234.5:c.2526G>A	ENSP00000418646.1:p.Glu842=
ENST00000482320.5:c.2520G>A	ENSP00000420089.1:p.Glu840=
ENST00000627585.2:c.2820G>A	ENSP00000487231.1:p.Glu940=
XM_011515989.1:c.2520G>A	XP_011514291.1:p.Glu840=