Canonical Allele Identifier: CA134942060

Gene: NUP153

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.17699091G>A , CM000668.2:g.17699091G>A	GRCh38
NC_000006.11:g.17699322G>A , CM000668.1:g.17699322G>A	GRCh37
NC_000006.10:g.17807301G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262077.3:c.111+7186C>T MANE Select	ENSP00000262077.3:n.111+7186C>T
ENST00000262077.2:c.111+7186C>T	ENSP00000262077.2:n.111+7186C>T
ENST00000537253.5:c.111+7186C>T	ENSP00000444029.1:n.111+7186C>T
ENST00000613258.4:c.111+7186C>T	ENSP00000478627.1:n.111+7186C>T
NM_001278209.1:c.111+7186C>T	NP_001265138.1:n.111+7186C>T
NM_001278210.1:c.111+7186C>T	NP_001265139.1:n.111+7186C>T
NM_005124.3:c.111+7186C>T	NP_005115.2:n.111+7186C>T
XM_005249507.1:c.111+7186C>T	XP_005249564.1:n.111+7186C>T
XM_006715290.1:c.111+7186C>T	XP_006715353.1:n.111+7186C>T
XM_006715291.2:c.111+7186C>T	XP_006715354.1:n.111+7186C>T
XM_011515028.1:c.111+7186C>T	XP_011513330.1:n.111+7186C>T
XM_005249507.3:c.111+7186C>T	XP_005249564.1:n.111+7186C>T
XM_006715290.3:c.111+7186C>T	XP_006715353.1:n.111+7186C>T
XM_006715291.4:c.111+7186C>T	XP_006715354.1:n.111+7186C>T
XM_011515028.3:c.111+7186C>T	XP_011513330.1:n.111+7186C>T
XM_017011594.2:c.111+7186C>T	XP_016867083.1:n.111+7186C>T
NM_005124.4:c.111+7186C>T MANE Select	NP_005115.2:n.111+7186C>T
NM_001278209.2:c.111+7186C>T	NP_001265138.1:n.111+7186C>T
NM_001278210.2:c.111+7186C>T	NP_001265139.1:n.111+7186C>T