Canonical Allele Identifier: CA2684841405

Gene: TNPO3

Linked Data

• gnomAD v4: 7-128954266-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128954266C>A , CM000669.2:g.128954266C>A	GRCh38
NC_000007.13:g.128594320C>A , CM000669.1:g.128594320C>A	GRCh37
NC_000007.12:g.128381556C>A	NCBI36
NG_023428.1:g.105908G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265388.10:c.*1151G>T MANE Select	ENSP00000265388.5:n.*1151G>T
ENST00000265388.9:c.*1151G>T	ENSP00000265388.5:n.*1151G>T
ENST00000627585.2:c.*1151G>T	ENSP00000487231.1:n.*1151G>T
NM_001191028.2:c.*1151G>T	NP_001177957.2:n.*1151G>T
NM_012470.3:c.*1151G>T	NP_036602.1:n.*1151G>T
NR_034053.2:n.4487G>T
XM_011515989.1:c.*1151G>T	XP_011514291.1:n.*1151G>T
NM_001191028.3:c.*1151G>T	NP_001177957.2:n.*1151G>T
NM_001382216.1:c.*1151G>T	NP_001369145.1:n.*1151G>T
NM_001382217.1:c.*1151G>T	NP_001369146.1:n.*1151G>T
NM_001382218.1:c.*1101G>T	NP_001369147.1:n.*1101G>T
NM_001382219.1:c.*1151G>T	NP_001369148.1:n.*1151G>T
NM_001382220.1:c.*1151G>T	NP_001369149.1:n.*1151G>T
NM_001382221.1:c.*1151G>T	NP_001369150.1:n.*1151G>T
NM_001382222.1:c.*1151G>T	NP_001369151.1:n.*1151G>T
NM_001382223.1:c.*1101G>T	NP_001369152.1:n.*1101G>T
NM_012470.4:c.*1151G>T MANE Select	NP_036602.1:n.*1151G>T
NR_034053.3:n.4425G>T
NR_167911.1:n.4512G>T
NR_167912.1:n.4370G>T
NR_167913.1:n.4172G>T
NR_167914.1:n.4332G>T
NR_167915.1:n.4588G>T
NR_167916.1:n.4062G>T
NR_167917.1:n.4095G>T
NR_167918.1:n.4550G>T
NR_167919.1:n.4389G>T
NR_167920.1:n.4348G>T
NR_167921.1:n.4550G>T
NR_167922.1:n.4386G>T
NR_167923.1:n.4187G>T
NR_167924.1:n.4415G>T
NR_167925.1:n.4187G>T
NR_167926.1:n.4198G>T
NR_167927.1:n.4491G>T