Canonical Allele Identifier: CA2684841400

Gene: TNPO3

Linked Data

• gnomAD v4: 7-128954225-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128954225G>T , CM000669.2:g.128954225G>T	GRCh38
NC_000007.13:g.128594279G>T , CM000669.1:g.128594279G>T	GRCh37
NC_000007.12:g.128381515G>T	NCBI36
NG_023428.1:g.105949C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265388.10:c.*1192C>A MANE Select	ENSP00000265388.5:n.*1192C>A
ENST00000265388.9:c.*1192C>A	ENSP00000265388.5:n.*1192C>A
ENST00000627585.2:c.*1192C>A	ENSP00000487231.1:n.*1192C>A
NM_001191028.2:c.*1192C>A	NP_001177957.2:n.*1192C>A
NM_012470.3:c.*1192C>A	NP_036602.1:n.*1192C>A
NR_034053.2:n.4528C>A
XM_011515989.1:c.*1192C>A	XP_011514291.1:n.*1192C>A
NM_001191028.3:c.*1192C>A	NP_001177957.2:n.*1192C>A
NM_001382216.1:c.*1192C>A	NP_001369145.1:n.*1192C>A
NM_001382217.1:c.*1192C>A	NP_001369146.1:n.*1192C>A
NM_001382218.1:c.*1142C>A	NP_001369147.1:n.*1142C>A
NM_001382219.1:c.*1192C>A	NP_001369148.1:n.*1192C>A
NM_001382220.1:c.*1192C>A	NP_001369149.1:n.*1192C>A
NM_001382221.1:c.*1192C>A	NP_001369150.1:n.*1192C>A
NM_001382222.1:c.*1192C>A	NP_001369151.1:n.*1192C>A
NM_001382223.1:c.*1142C>A	NP_001369152.1:n.*1142C>A
NM_012470.4:c.*1192C>A MANE Select	NP_036602.1:n.*1192C>A
NR_034053.3:n.4466C>A
NR_167911.1:n.4553C>A
NR_167912.1:n.4411C>A
NR_167913.1:n.4213C>A
NR_167914.1:n.4373C>A
NR_167915.1:n.4629C>A
NR_167916.1:n.4103C>A
NR_167917.1:n.4136C>A
NR_167918.1:n.4591C>A
NR_167919.1:n.4430C>A
NR_167920.1:n.4389C>A
NR_167921.1:n.4591C>A
NR_167922.1:n.4427C>A
NR_167923.1:n.4228C>A
NR_167924.1:n.4456C>A
NR_167925.1:n.4228C>A
NR_167926.1:n.4239C>A
NR_167927.1:n.4532C>A