Canonical Allele Identifier: CA1742576287

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128954250A= , CM000669.2:g.128954250A=	GRCh38
NC_000007.13:g.128594304A= , CM000669.1:g.128594304A=	GRCh37
NC_000007.12:g.128381540A=	NCBI36
NG_023428.1:g.105924T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265388.10:c.*1167T= MANE Select	ENSP00000265388.5:n.*1167T=
ENST00000265388.9:c.*1167T=	ENSP00000265388.5:n.*1167T=
ENST00000627585.2:c.*1167T=	ENSP00000487231.1:n.*1167T=
NM_001191028.2:c.*1167T=	NP_001177957.2:n.*1167T=
NM_012470.3:c.*1167T=	NP_036602.1:n.*1167T=
NR_034053.2:n.4503T=
XM_011515989.1:c.*1167T=	XP_011514291.1:n.*1167T=
NM_001191028.3:c.*1167T=	NP_001177957.2:n.*1167T=
NM_001382216.1:c.*1167T=	NP_001369145.1:n.*1167T=
NM_001382217.1:c.*1167T=	NP_001369146.1:n.*1167T=
NM_001382218.1:c.*1117T=	NP_001369147.1:n.*1117T=
NM_001382219.1:c.*1167T=	NP_001369148.1:n.*1167T=
NM_001382220.1:c.*1167T=	NP_001369149.1:n.*1167T=
NM_001382221.1:c.*1167T=	NP_001369150.1:n.*1167T=
NM_001382222.1:c.*1167T=	NP_001369151.1:n.*1167T=
NM_001382223.1:c.*1117T=	NP_001369152.1:n.*1117T=
NM_012470.4:c.*1167T= MANE Select	NP_036602.1:n.*1167T=
NR_034053.3:n.4441T=
NR_167911.1:n.4528T=
NR_167912.1:n.4386T=
NR_167913.1:n.4188T=
NR_167914.1:n.4348T=
NR_167915.1:n.4604T=
NR_167916.1:n.4078T=
NR_167917.1:n.4111T=
NR_167918.1:n.4566T=
NR_167919.1:n.4405T=
NR_167920.1:n.4364T=
NR_167921.1:n.4566T=
NR_167922.1:n.4402T=
NR_167923.1:n.4203T=
NR_167924.1:n.4431T=
NR_167925.1:n.4203T=
NR_167926.1:n.4214T=
NR_167927.1:n.4507T=