Canonical Allele Identifier: CA2838283412

Gene: NUP205

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.135593270dup , CM000669.2:g.135593270dup	GRCh38
NC_000007.13:g.135278018dup , CM000669.1:g.135278018dup	GRCh37
NC_000007.12:g.134928558dup	NCBI36
NG_051184.1:g.40357dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285968.11:c.1830+78dup MANE Select	ENSP00000285968.6:n.1830+78dup
ENST00000285968.10:c.1830+78dup	ENSP00000285968.6:n.1830+78dup
NM_015135.2:c.1830+78dup	NP_055950.1:n.1830+78dup
XM_005250235.2:c.756+78dup	XP_005250292.1:n.756+78dup
NM_001329434.1:c.756+78dup	NP_001316363.1:n.756+78dup
NM_015135.3:c.1830+78dup MANE Select	NP_055950.2:n.1830+78dup
NM_001329434.2:c.756+78dup	NP_001316363.2:n.756+78dup