Canonical Allele Identifier: CA1742576231

Gene: TNPO3

Linked Data

• dbSNP Id: rs1796705403

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128954199T>C , CM000669.2:g.128954199T>C	GRCh38
NC_000007.13:g.128594253T>C , CM000669.1:g.128594253T>C	GRCh37
NC_000007.12:g.128381489T>C	NCBI36
NG_023428.1:g.105975A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265388.10:c.*1218A>G MANE Select	ENSP00000265388.5:n.*1218A>G
ENST00000265388.9:c.*1218A>G	ENSP00000265388.5:n.*1218A>G
ENST00000627585.2:c.*1218A>G	ENSP00000487231.1:n.*1218A>G
NM_001191028.2:c.*1218A>G	NP_001177957.2:n.*1218A>G
NM_012470.3:c.*1218A>G	NP_036602.1:n.*1218A>G
NR_034053.2:n.4554A>G
XM_011515989.1:c.*1218A>G	XP_011514291.1:n.*1218A>G
NM_001191028.3:c.*1218A>G	NP_001177957.2:n.*1218A>G
NM_001382216.1:c.*1218A>G	NP_001369145.1:n.*1218A>G
NM_001382217.1:c.*1218A>G	NP_001369146.1:n.*1218A>G
NM_001382218.1:c.*1168A>G	NP_001369147.1:n.*1168A>G
NM_001382219.1:c.*1218A>G	NP_001369148.1:n.*1218A>G
NM_001382220.1:c.*1218A>G	NP_001369149.1:n.*1218A>G
NM_001382221.1:c.*1218A>G	NP_001369150.1:n.*1218A>G
NM_001382222.1:c.*1218A>G	NP_001369151.1:n.*1218A>G
NM_001382223.1:c.*1168A>G	NP_001369152.1:n.*1168A>G
NM_012470.4:c.*1218A>G MANE Select	NP_036602.1:n.*1218A>G
NR_034053.3:n.4492A>G
NR_167911.1:n.4579A>G
NR_167912.1:n.4437A>G
NR_167913.1:n.4239A>G
NR_167914.1:n.4399A>G
NR_167915.1:n.4655A>G
NR_167916.1:n.4129A>G
NR_167917.1:n.4162A>G
NR_167918.1:n.4617A>G
NR_167919.1:n.4456A>G
NR_167920.1:n.4415A>G
NR_167921.1:n.4617A>G
NR_167922.1:n.4453A>G
NR_167923.1:n.4254A>G
NR_167924.1:n.4482A>G
NR_167925.1:n.4254A>G
NR_167926.1:n.4265A>G
NR_167927.1:n.4558A>G