Canonical Allele Identifier: CA4477851

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128970201T>C , CM000669.2:g.128970201T>C	GRCh38
NC_000007.13:g.128610255T>C , CM000669.1:g.128610255T>C	GRCh37
NC_000007.12:g.128397491T>C	NCBI36
NG_023428.1:g.89973A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012470.4:c.2545A>G MANE Select	NP_036602.1:p.Thr849Ala
ENST00000265388.10:c.2545A>G MANE Select	ENSP00000265388.5:p.Thr849Ala
NM_001191028.2:c.2353A>G	NP_001177957.2:p.Thr785Ala
NM_001191028.3:c.2353A>G	NP_001177957.2:p.Thr785Ala
NM_001382216.1:c.2647A>G	NP_001369145.1:p.Thr883Ala
NM_001382217.1:c.2626A>G	NP_001369146.1:p.Thr876Ala
NM_001382218.1:c.2545A>G	NP_001369147.1:p.Thr849Ala
NM_001382219.1:c.2437A>G	NP_001369148.1:p.Thr813Ala
NM_001382220.1:c.2404A>G	NP_001369149.1:p.Thr802Ala
NM_001382221.1:c.2401A>G	NP_001369150.1:p.Thr801Ala
NM_001382222.1:c.2398A>G	NP_001369151.1:p.Thr800Ala
NM_001382223.1:c.2353A>G	NP_001369152.1:p.Thr785Ala
NM_012470.3:c.2545A>G	NP_036602.1:p.Thr849Ala
NR_034053.2:n.3109A>G
NR_034053.3:n.3047A>G
NR_167911.1:n.3134A>G
NR_167912.1:n.2992A>G
NR_167913.1:n.2794A>G
NR_167914.1:n.2954A>G
NR_167915.1:n.3210A>G
NR_167916.1:n.2684A>G
NR_167917.1:n.2717A>G
NR_167918.1:n.3172A>G
NR_167919.1:n.3011A>G
NR_167920.1:n.2970A>G
NR_167921.1:n.3172A>G
NR_167922.1:n.3008A>G
NR_167923.1:n.2809A>G
NR_167924.1:n.2886A>G
NR_167925.1:n.2809A>G
NR_167926.1:n.2820A>G
NR_167927.1:n.3113A>G
ENST00000265388.9:c.2545A>G	ENSP00000265388.5:p.Thr849Ala
ENST00000471166.1:c.2647A>G	ENSP00000418267.1:p.Thr883Ala
ENST00000471234.5:c.2353A>G	ENSP00000418646.1:p.Thr785Ala
ENST00000482320.5:c.2347A>G	ENSP00000420089.1:p.Thr783Ala
ENST00000627585.2:c.2647A>G	ENSP00000487231.1:p.Thr883Ala
XM_011515989.1:c.2347A>G	XP_011514291.1:p.Thr783Ala