Canonical Allele Identifier: CA4478295
Gene: TNPO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 389221
dbSNP Id: rs780935123

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129000570G>A , CM000669.2:g.129000570G>A GRCh38
NC_000007.13:g.128640624G>A , CM000669.1:g.128640624G>A GRCh37
NC_000007.12:g.128427860G>A NCBI36
NG_023428.1:g.59604C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265388.10:c.873-3C>T MANE Select ENSP00000265388.5:n.873-3C>T
ENST00000265388.9:c.873-3C>T ENSP00000265388.5:n.873-3C>T
ENST00000471166.1:c.873-3C>T ENSP00000418267.1:n.873-3C>T
ENST00000471234.5:c.873-3C>T ENSP00000418646.1:n.873-3C>T
ENST00000482320.5:c.675-3C>T ENSP00000420089.1:n.675-3C>T
ENST00000627585.2:c.873-3C>T ENSP00000487231.1:n.873-3C>T
NM_001191028.2:c.873-3C>T NP_001177957.2:n.873-3C>T
NM_012470.3:c.873-3C>T NP_036602.1:n.873-3C>T
NR_034053.2:n.1437-3C>T
XM_011515989.1:c.675-3C>T XP_011514291.1:n.675-3C>T
NM_001191028.3:c.873-3C>T NP_001177957.2:n.873-3C>T
NM_001382216.1:c.873-3C>T NP_001369145.1:n.873-3C>T
NM_001382217.1:c.954-3C>T NP_001369146.1:n.954-3C>T
NM_001382218.1:c.873-3C>T NP_001369147.1:n.873-3C>T
NM_001382219.1:c.873-3C>T NP_001369148.1:n.873-3C>T
NM_001382220.1:c.873-3C>T NP_001369149.1:n.873-3C>T
NM_001382221.1:c.729-3C>T NP_001369150.1:n.729-3C>T
NM_001382222.1:c.873-3C>T NP_001369151.1:n.873-3C>T
NM_001382223.1:c.873-3C>T NP_001369152.1:n.873-3C>T
NM_012470.4:c.873-3C>T MANE Select NP_036602.1:n.873-3C>T
NR_034053.3:n.1375-3C>T
NR_167911.1:n.1462-3C>T
NR_167912.1:n.1214-3C>T
NR_167913.1:n.1214-3C>T
NR_167914.1:n.1214-3C>T
NR_167915.1:n.1375-3C>T
NR_167916.1:n.1214-3C>T
NR_167917.1:n.1214-3C>T
NR_167918.1:n.1500-3C>T
NR_167919.1:n.1339-3C>T
NR_167920.1:n.1500-3C>T
NR_167921.1:n.1500-3C>T
NR_167922.1:n.1336-3C>T
NR_167923.1:n.1339-3C>T
NR_167924.1:n.1214-3C>T
NR_167925.1:n.1214-3C>T
NR_167926.1:n.1497-3C>T
NR_167927.1:n.1339-3C>T