Canonical Allele Identifier: CA833146243

Gene: TNPO3

Linked Data

• dbSNP Id: rs1299410640
• gnomAD v3: 7-128954189-A-G
• gnomAD v4: 7-128954189-A-G
• MyVariant Identifiers: chr7:g.128594243A>G (hg19) ; chr7:g.128954189A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128954189A>G , CM000669.2:g.128954189A>G	GRCh38
NC_000007.13:g.128594243A>G , CM000669.1:g.128594243A>G	GRCh37
NC_000007.12:g.128381479A>G	NCBI36
NG_023428.1:g.105985T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265388.10:c.*1228T>C MANE Select	ENSP00000265388.5:n.*1228T>C
ENST00000265388.9:c.*1228T>C	ENSP00000265388.5:n.*1228T>C
ENST00000627585.2:c.*1228T>C	ENSP00000487231.1:n.*1228T>C
NM_001191028.2:c.*1228T>C	NP_001177957.2:n.*1228T>C
NM_012470.3:c.*1228T>C	NP_036602.1:n.*1228T>C
NR_034053.2:n.4564T>C
XM_011515989.1:c.*1228T>C	XP_011514291.1:n.*1228T>C
NM_001191028.3:c.*1228T>C	NP_001177957.2:n.*1228T>C
NM_001382216.1:c.*1228T>C	NP_001369145.1:n.*1228T>C
NM_001382217.1:c.*1228T>C	NP_001369146.1:n.*1228T>C
NM_001382218.1:c.*1178T>C	NP_001369147.1:n.*1178T>C
NM_001382219.1:c.*1228T>C	NP_001369148.1:n.*1228T>C
NM_001382220.1:c.*1228T>C	NP_001369149.1:n.*1228T>C
NM_001382221.1:c.*1228T>C	NP_001369150.1:n.*1228T>C
NM_001382222.1:c.*1228T>C	NP_001369151.1:n.*1228T>C
NM_001382223.1:c.*1178T>C	NP_001369152.1:n.*1178T>C
NM_012470.4:c.*1228T>C MANE Select	NP_036602.1:n.*1228T>C
NR_034053.3:n.4502T>C
NR_167911.1:n.4589T>C
NR_167912.1:n.4447T>C
NR_167913.1:n.4249T>C
NR_167914.1:n.4409T>C
NR_167915.1:n.4665T>C
NR_167916.1:n.4139T>C
NR_167917.1:n.4172T>C
NR_167918.1:n.4627T>C
NR_167919.1:n.4466T>C
NR_167920.1:n.4425T>C
NR_167921.1:n.4627T>C
NR_167922.1:n.4463T>C
NR_167923.1:n.4264T>C
NR_167924.1:n.4492T>C
NR_167925.1:n.4264T>C
NR_167926.1:n.4275T>C
NR_167927.1:n.4568T>C