Canonical Allele Identifier: CA2840006085

Gene: NUP205

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.135645429dup , CM000669.2:g.135645429dup	GRCh38
NC_000007.13:g.135330177dup , CM000669.1:g.135330177dup	GRCh37
NC_000007.12:g.134980717dup	NCBI36
NG_051184.1:g.92516dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285968.11:c.5684-39dup MANE Select	ENSP00000285968.6:n.5684-39dup
ENST00000285968.10:c.5684-39dup	ENSP00000285968.6:n.5684-39dup
ENST00000461255.5:n.891-39dup
ENST00000477620.5:c.1405+451dup
ENST00000490439.1:c.121-412dup
ENST00000607647.5:n.3962-39dup
NM_015135.2:c.5684-39dup	NP_055950.1:n.5684-39dup
XM_005250235.2:c.4610-39dup	XP_005250292.1:n.4610-39dup
NM_001329434.1:c.4610-39dup	NP_001316363.1:n.4610-39dup
NM_015135.3:c.5684-39dup MANE Select	NP_055950.2:n.5684-39dup
NM_001329434.2:c.4610-39dup	NP_001316363.2:n.4610-39dup