Canonical Allele Identifier: CA166207770
Gene: TNPO3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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