Canonical Allele Identifier: CA2684841395

Gene: TNPO3

Linked Data

• gnomAD v4: 7-128954192-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128954192T>G , CM000669.2:g.128954192T>G	GRCh38
NC_000007.13:g.128594246T>G , CM000669.1:g.128594246T>G	GRCh37
NC_000007.12:g.128381482T>G	NCBI36
NG_023428.1:g.105982A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265388.10:c.*1225A>C MANE Select	ENSP00000265388.5:n.*1225A>C
ENST00000265388.9:c.*1225A>C	ENSP00000265388.5:n.*1225A>C
ENST00000627585.2:c.*1225A>C	ENSP00000487231.1:n.*1225A>C
NM_001191028.2:c.*1225A>C	NP_001177957.2:n.*1225A>C
NM_012470.3:c.*1225A>C	NP_036602.1:n.*1225A>C
NR_034053.2:n.4561A>C
XM_011515989.1:c.*1225A>C	XP_011514291.1:n.*1225A>C
NM_001191028.3:c.*1225A>C	NP_001177957.2:n.*1225A>C
NM_001382216.1:c.*1225A>C	NP_001369145.1:n.*1225A>C
NM_001382217.1:c.*1225A>C	NP_001369146.1:n.*1225A>C
NM_001382218.1:c.*1175A>C	NP_001369147.1:n.*1175A>C
NM_001382219.1:c.*1225A>C	NP_001369148.1:n.*1225A>C
NM_001382220.1:c.*1225A>C	NP_001369149.1:n.*1225A>C
NM_001382221.1:c.*1225A>C	NP_001369150.1:n.*1225A>C
NM_001382222.1:c.*1225A>C	NP_001369151.1:n.*1225A>C
NM_001382223.1:c.*1175A>C	NP_001369152.1:n.*1175A>C
NM_012470.4:c.*1225A>C MANE Select	NP_036602.1:n.*1225A>C
NR_034053.3:n.4499A>C
NR_167911.1:n.4586A>C
NR_167912.1:n.4444A>C
NR_167913.1:n.4246A>C
NR_167914.1:n.4406A>C
NR_167915.1:n.4662A>C
NR_167916.1:n.4136A>C
NR_167917.1:n.4169A>C
NR_167918.1:n.4624A>C
NR_167919.1:n.4463A>C
NR_167920.1:n.4422A>C
NR_167921.1:n.4624A>C
NR_167922.1:n.4460A>C
NR_167923.1:n.4261A>C
NR_167924.1:n.4489A>C
NR_167925.1:n.4261A>C
NR_167926.1:n.4272A>C
NR_167927.1:n.4565A>C