Canonical Allele Identifier: CA9229310

Gene: TNPO2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12715329C>T , CM000681.2:g.12715329C>T	GRCh38
NC_000019.9:g.12826143C>T , CM000681.1:g.12826143C>T	GRCh37
NC_000019.8:g.12687143C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001382241.1:c.567-5G>A MANE Select	NP_001369170.1:n.567-5G>A
ENST00000425528.6:c.567-5G>A MANE Select	ENSP00000407182.1:n.567-5G>A
NM_001136195.1:c.567-5G>A	NP_001129667.1:n.567-5G>A
NM_001136195.2:c.567-5G>A	NP_001129667.1:n.567-5G>A
NM_001136196.1:c.567-5G>A	NP_001129668.1:n.567-5G>A
NM_001136196.2:c.567-5G>A	NP_001129668.1:n.567-5G>A
NM_001382236.1:c.567-5G>A	NP_001369165.1:n.567-5G>A
NM_001382237.1:c.567-5G>A	NP_001369166.1:n.567-5G>A
NM_001382238.1:c.567-5G>A	NP_001369167.1:n.567-5G>A
NM_001382239.1:c.567-5G>A	NP_001369168.1:n.567-5G>A
NM_001382240.1:c.567-5G>A	NP_001369169.1:n.567-5G>A
NM_001382242.1:c.567-5G>A	NP_001369171.1:n.567-5G>A
NM_001382243.1:c.567-5G>A	NP_001369172.1:n.567-5G>A
NM_013433.4:c.567-5G>A	NP_038461.2:n.567-5G>A
NM_013433.5:c.567-5G>A	NP_038461.2:n.567-5G>A
NR_167974.1:n.706-5G>A
NR_167975.1:n.861-5G>A
NR_167976.1:n.832-5G>A
NR_167977.1:n.832-5G>A
NR_167978.1:n.664-5G>A
NR_167979.1:n.677-5G>A
ENST00000356861.9:c.567-5G>A	ENSP00000349321.4:n.567-5G>A
ENST00000425528.5:c.567-5G>A	ENSP00000407182.1:n.567-5G>A
ENST00000450764.6:c.567-5G>A	ENSP00000397379.2:n.567-5G>A
ENST00000585886.5:c.567-5G>A	ENSP00000468101.1:n.567-5G>A
ENST00000586775.5:c.*208-5G>A	ENSP00000466446.1:n.*208-5G>A
ENST00000588216.5:c.567-5G>A	ENSP00000465625.1:n.567-5G>A
ENST00000588484.1:n.419-5G>A
ENST00000589956.5:n.432+381G>A
ENST00000592287.5:c.567-5G>A	ENSP00000468434.1:n.567-5G>A