Canonical Allele Identifier: CA2685060108

Gene: NUP205

Linked Data

• gnomAD v4: 7-135645084-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.135645087_135645088del , CM000669.2:g.135645087_135645088del	GRCh38
NC_000007.13:g.135329835_135329836del , CM000669.1:g.135329835_135329836del	GRCh37
NC_000007.12:g.134980375_134980376del	NCBI36
NG_051184.1:g.92174_92175del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285968.11:c.5683+69_5683+70del MANE Select	ENSP00000285968.6:n.5683+69_5683+70del
ENST00000285968.10:c.5683+69_5683+70del	ENSP00000285968.6:n.5683+69_5683+70del
ENST00000461255.5:n.890+69_890+70del
ENST00000477620.5:c.1405+109_1405+110del
ENST00000490439.1:c.120+69_120+70del
ENST00000607647.5:n.3961+69_3961+70del
NM_015135.2:c.5683+69_5683+70del	NP_055950.1:n.5683+69_5683+70del
XM_005250235.2:c.4609+69_4609+70del	XP_005250292.1:n.4609+69_4609+70del
NM_001329434.1:c.4609+69_4609+70del	NP_001316363.1:n.4609+69_4609+70del
NM_015135.3:c.5683+69_5683+70del MANE Select	NP_055950.2:n.5683+69_5683+70del
NM_001329434.2:c.4609+69_4609+70del	NP_001316363.2:n.4609+69_4609+70del