Canonical Allele Identifier: CA166207761
Gene: TNPO3 HGNC NCBI

Linked Data

dbSNP Id: rs12531711

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128977412A>C , CM000669.2:g.128977412A>C GRCh38
NC_000007.13:g.128617466A>C , CM000669.1:g.128617466A>C GRCh37
NC_000007.12:g.128404702A>C NCBI36
NG_023428.1:g.82762T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265388.10:c.2062-1477T>G MANE Select ENSP00000265388.5:n.2062-1477T>G
ENST00000265388.9:c.2062-1477T>G ENSP00000265388.5:n.2062-1477T>G
ENST00000471166.1:c.2164-1477T>G ENSP00000418267.1:n.2164-1477T>G
ENST00000471234.5:c.1870-1477T>G ENSP00000418646.1:n.1870-1477T>G
ENST00000482320.5:c.1864-1477T>G ENSP00000420089.1:n.1864-1477T>G
ENST00000627585.2:c.2164-1477T>G ENSP00000487231.1:n.2164-1477T>G
NM_001191028.2:c.1870-1477T>G NP_001177957.2:n.1870-1477T>G
NM_012470.3:c.2062-1477T>G NP_036602.1:n.2062-1477T>G
NR_034053.2:n.2626-1477T>G
XM_011515989.1:c.1864-1477T>G XP_011514291.1:n.1864-1477T>G
NM_001191028.3:c.1870-1477T>G NP_001177957.2:n.1870-1477T>G
NM_001382216.1:c.2164-1477T>G NP_001369145.1:n.2164-1477T>G
NM_001382217.1:c.2143-1477T>G NP_001369146.1:n.2143-1477T>G
NM_001382218.1:c.2062-1477T>G NP_001369147.1:n.2062-1477T>G
NM_001382219.1:c.1954-1477T>G NP_001369148.1:n.1954-1477T>G
NM_001382220.1:c.1921-1477T>G NP_001369149.1:n.1921-1477T>G
NM_001382221.1:c.1918-1477T>G NP_001369150.1:n.1918-1477T>G
NM_001382222.1:c.1915-1477T>G NP_001369151.1:n.1915-1477T>G
NM_001382223.1:c.1870-1477T>G NP_001369152.1:n.1870-1477T>G
NM_012470.4:c.2062-1477T>G MANE Select NP_036602.1:n.2062-1477T>G
NR_034053.3:n.2564-1477T>G
NR_167911.1:n.2651-1477T>G
NR_167912.1:n.2509-1477T>G
NR_167913.1:n.2311-1477T>G
NR_167914.1:n.2471-1477T>G
NR_167915.1:n.2564-1477T>G
NR_167916.1:n.2201-1477T>G
NR_167917.1:n.2234-1477T>G
NR_167918.1:n.2689-1477T>G
NR_167919.1:n.2528-1477T>G
NR_167920.1:n.2487-1477T>G
NR_167921.1:n.2689-1477T>G
NR_167922.1:n.2525-1477T>G
NR_167923.1:n.2326-1477T>G
NR_167924.1:n.2403-1477T>G
NR_167925.1:n.2326-1477T>G
NR_167926.1:n.2337-1477T>G
NR_167927.1:n.2630-1477T>G