Canonical Allele Identifier: CA5981495

Gene: NUP160

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47835824_47835825dup , CM000673.2:g.47835824_47835825dup	GRCh38
NC_000011.9:g.47857376_47857377dup , CM000673.1:g.47857376_47857377dup	GRCh37
NC_000011.8:g.47813952_47813953dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015231.3:c.841-16_841-15dup MANE Select	NP_056046.2:n.841-16_841-15dup
ENST00000378460.7:c.841-16_841-15dup MANE Select	ENSP00000367721.3:n.841-16_841-15dup
NM_015231.1:c.943-16_943-15dup	NP_056046.1:n.943-16_943-15dup
NM_015231.2:c.943-16_943-15dup	NP_056046.1:n.943-16_943-15dup
NR_134636.1:n.1067-16_1067-15dup
NR_134636.2:n.873-16_873-15dup
NR_134636.3:n.873-16_873-15dup
ENST00000378460.6:c.943-16_943-15dup	ENSP00000367721.2:n.943-16_943-15dup
ENST00000528071.5:c.857-16_857-15dup
ENST00000528501.5:c.419-16_419-15dup	ENSP00000433964.2:n.419-16_419-15dup
ENST00000530326.5:c.836-16_836-15dup
ENST00000694866.1:c.943-16_943-15dup	ENSP00000511549.1:n.943-16_943-15dup
XM_006718170.2:c.-1035-16_-1035-15dup	XP_006718233.1:n.-1035-16_-1035-15dup