Canonical Allele Identifier: CA4477880

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128972443T>C , CM000669.2:g.128972443T>C	GRCh38
NC_000007.13:g.128612497T>C , CM000669.1:g.128612497T>C	GRCh37
NC_000007.12:g.128399733T>C	NCBI36
NG_023428.1:g.87731A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012470.4:c.2413A>G MANE Select	NP_036602.1:p.Thr805Ala
ENST00000265388.10:c.2413A>G MANE Select	ENSP00000265388.5:p.Thr805Ala
NM_001191028.2:c.2221A>G	NP_001177957.2:p.Thr741Ala
NM_001191028.3:c.2221A>G	NP_001177957.2:p.Thr741Ala
NM_001382216.1:c.2515A>G	NP_001369145.1:p.Thr839Ala
NM_001382217.1:c.2494A>G	NP_001369146.1:p.Thr832Ala
NM_001382218.1:c.2413A>G	NP_001369147.1:p.Thr805Ala
NM_001382219.1:c.2305A>G	NP_001369148.1:p.Thr769Ala
NM_001382220.1:c.2272A>G	NP_001369149.1:p.Thr758Ala
NM_001382221.1:c.2269A>G	NP_001369150.1:p.Thr757Ala
NM_001382222.1:c.2266A>G	NP_001369151.1:p.Thr756Ala
NM_001382223.1:c.2221A>G	NP_001369152.1:p.Thr741Ala
NM_012470.3:c.2413A>G	NP_036602.1:p.Thr805Ala
NR_034053.2:n.2977A>G
NR_034053.3:n.2915A>G
NR_167911.1:n.3002A>G
NR_167912.1:n.2860A>G
NR_167913.1:n.2662A>G
NR_167914.1:n.2822A>G
NR_167915.1:n.3078A>G
NR_167916.1:n.2552A>G
NR_167917.1:n.2585A>G
NR_167918.1:n.3040A>G
NR_167919.1:n.2879A>G
NR_167920.1:n.2838A>G
NR_167921.1:n.3040A>G
NR_167922.1:n.2876A>G
NR_167923.1:n.2677A>G
NR_167924.1:n.2754A>G
NR_167925.1:n.2677A>G
NR_167926.1:n.2688A>G
NR_167927.1:n.2981A>G
ENST00000265388.9:c.2413A>G	ENSP00000265388.5:p.Thr805Ala
ENST00000471166.1:c.2515A>G	ENSP00000418267.1:p.Thr839Ala
ENST00000471234.5:c.2221A>G	ENSP00000418646.1:p.Thr741Ala
ENST00000482320.5:c.2215A>G	ENSP00000420089.1:p.Thr739Ala
ENST00000627585.2:c.2515A>G	ENSP00000487231.1:p.Thr839Ala
XM_011515989.1:c.2215A>G	XP_011514291.1:p.Thr739Ala