Canonical Allele Identifier: CA4477820

Gene: TNPO3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128967366G>A , CM000669.2:g.128967366G>A	GRCh38
NC_000007.13:g.128607420G>A , CM000669.1:g.128607420G>A	GRCh37
NC_000007.12:g.128394656G>A	NCBI36
NG_023428.1:g.92808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265388.10:c.2625C>T MANE Select	ENSP00000265388.5:p.Ser875=
ENST00000265388.9:c.2625C>T	ENSP00000265388.5:p.Ser875=
ENST00000471166.1:c.2727C>T	ENSP00000418267.1:p.Ser909=
ENST00000471234.5:c.2433C>T	ENSP00000418646.1:p.Ser811=
ENST00000482320.5:c.2427C>T	ENSP00000420089.1:p.Ser809=
ENST00000627585.2:c.2727C>T	ENSP00000487231.1:p.Ser909=
NM_001191028.2:c.2433C>T	NP_001177957.2:p.Ser811=
NM_012470.3:c.2625C>T	NP_036602.1:p.Ser875=
NR_034053.2:n.3189C>T
XM_011515989.1:c.2427C>T	XP_011514291.1:p.Ser809=
NM_001191028.3:c.2433C>T	NP_001177957.2:p.Ser811=
NM_001382216.1:c.2727C>T	NP_001369145.1:p.Ser909=
NM_001382217.1:c.2706C>T	NP_001369146.1:p.Ser902=
NM_001382218.1:c.2625C>T	NP_001369147.1:p.Ser875=
NM_001382219.1:c.2517C>T	NP_001369148.1:p.Ser839=
NM_001382220.1:c.2484C>T	NP_001369149.1:p.Ser828=
NM_001382221.1:c.2481C>T	NP_001369150.1:p.Ser827=
NM_001382222.1:c.2478C>T	NP_001369151.1:p.Ser826=
NM_001382223.1:c.2433C>T	NP_001369152.1:p.Ser811=
NM_012470.4:c.2625C>T MANE Select	NP_036602.1:p.Ser875=
NR_034053.3:n.3127C>T
NR_167911.1:n.3214C>T
NR_167912.1:n.3072C>T
NR_167913.1:n.2874C>T
NR_167914.1:n.3034C>T
NR_167915.1:n.3290C>T
NR_167916.1:n.2764C>T
NR_167917.1:n.2797C>T
NR_167918.1:n.3252C>T
NR_167919.1:n.3091C>T
NR_167920.1:n.3050C>T
NR_167921.1:n.3252C>T
NR_167922.1:n.3088C>T
NR_167923.1:n.2889C>T
NR_167924.1:n.2966C>T
NR_167925.1:n.2889C>T
NR_167926.1:n.2900C>T
NR_167927.1:n.3193C>T