Canonical Allele Identifier: CA4477810

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128967283G>C , CM000669.2:g.128967283G>C	GRCh38
NC_000007.13:g.128607337G>C , CM000669.1:g.128607337G>C	GRCh37
NC_000007.12:g.128394573G>C	NCBI36
NG_023428.1:g.92891C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012470.4:c.2708C>G MANE Select	NP_036602.1:p.Thr903Ser
ENST00000265388.10:c.2708C>G MANE Select	ENSP00000265388.5:p.Thr903Ser
NM_001191028.2:c.2516C>G	NP_001177957.2:p.Thr839Ser
NM_001191028.3:c.2516C>G	NP_001177957.2:p.Thr839Ser
NM_001382216.1:c.2810C>G	NP_001369145.1:p.Thr937Ser
NM_001382217.1:c.2789C>G	NP_001369146.1:p.Thr930Ser
NM_001382218.1:c.2708C>G	NP_001369147.1:p.Thr903Ser
NM_001382219.1:c.2600C>G	NP_001369148.1:p.Thr867Ser
NM_001382220.1:c.2567C>G	NP_001369149.1:p.Thr856Ser
NM_001382221.1:c.2564C>G	NP_001369150.1:p.Thr855Ser
NM_001382222.1:c.2561C>G	NP_001369151.1:p.Thr854Ser
NM_001382223.1:c.2516C>G	NP_001369152.1:p.Thr839Ser
NM_012470.3:c.2708C>G	NP_036602.1:p.Thr903Ser
NR_034053.2:n.3272C>G
NR_034053.3:n.3210C>G
NR_167911.1:n.3297C>G
NR_167912.1:n.3155C>G
NR_167913.1:n.2957C>G
NR_167914.1:n.3117C>G
NR_167915.1:n.3373C>G
NR_167916.1:n.2847C>G
NR_167917.1:n.2880C>G
NR_167918.1:n.3335C>G
NR_167919.1:n.3174C>G
NR_167920.1:n.3133C>G
NR_167921.1:n.3335C>G
NR_167922.1:n.3171C>G
NR_167923.1:n.2972C>G
NR_167924.1:n.3049C>G
NR_167925.1:n.2972C>G
NR_167926.1:n.2983C>G
NR_167927.1:n.3276C>G
ENST00000265388.9:c.2708C>G	ENSP00000265388.5:p.Thr903Ser
ENST00000471166.1:c.2810C>G	ENSP00000418267.1:p.Thr937Ser
ENST00000471234.5:c.2516C>G	ENSP00000418646.1:p.Thr839Ser
ENST00000482320.5:c.2510C>G	ENSP00000420089.1:p.Thr837Ser
ENST00000627585.2:c.2810C>G	ENSP00000487231.1:p.Thr937Ser
XM_011515989.1:c.2510C>G	XP_011514291.1:p.Thr837Ser