Canonical Allele Identifier: CA833146230

Gene: TNPO3

Linked Data

• dbSNP Id: rs1365440396
• MyVariant Identifiers: chr7:g.128594239T>C (hg19) ; chr7:g.128954185T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128954185T>C , CM000669.2:g.128954185T>C	GRCh38
NC_000007.13:g.128594239T>C , CM000669.1:g.128594239T>C	GRCh37
NC_000007.12:g.128381475T>C	NCBI36
NG_023428.1:g.105989A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265388.10:c.*1232A>G MANE Select	ENSP00000265388.5:n.*1232A>G
ENST00000265388.9:c.*1232A>G	ENSP00000265388.5:n.*1232A>G
ENST00000627585.2:c.*1232A>G	ENSP00000487231.1:n.*1232A>G
NM_001191028.2:c.*1232A>G	NP_001177957.2:n.*1232A>G
NM_012470.3:c.*1232A>G	NP_036602.1:n.*1232A>G
NR_034053.2:n.4568A>G
XM_011515989.1:c.*1232A>G	XP_011514291.1:n.*1232A>G
NM_001191028.3:c.*1232A>G	NP_001177957.2:n.*1232A>G
NM_001382216.1:c.*1232A>G	NP_001369145.1:n.*1232A>G
NM_001382217.1:c.*1232A>G	NP_001369146.1:n.*1232A>G
NM_001382218.1:c.*1182A>G	NP_001369147.1:n.*1182A>G
NM_001382219.1:c.*1232A>G	NP_001369148.1:n.*1232A>G
NM_001382220.1:c.*1232A>G	NP_001369149.1:n.*1232A>G
NM_001382221.1:c.*1232A>G	NP_001369150.1:n.*1232A>G
NM_001382222.1:c.*1232A>G	NP_001369151.1:n.*1232A>G
NM_001382223.1:c.*1182A>G	NP_001369152.1:n.*1182A>G
NM_012470.4:c.*1232A>G MANE Select	NP_036602.1:n.*1232A>G
NR_034053.3:n.4506A>G
NR_167911.1:n.4593A>G
NR_167912.1:n.4451A>G
NR_167913.1:n.4253A>G
NR_167914.1:n.4413A>G
NR_167915.1:n.4669A>G
NR_167916.1:n.4143A>G
NR_167917.1:n.4176A>G
NR_167918.1:n.4631A>G
NR_167919.1:n.4470A>G
NR_167920.1:n.4429A>G
NR_167921.1:n.4631A>G
NR_167922.1:n.4467A>G
NR_167923.1:n.4268A>G
NR_167924.1:n.4496A>G
NR_167925.1:n.4268A>G
NR_167926.1:n.4279A>G
NR_167927.1:n.4572A>G