Canonical Allele Identifier: CA167066880
Gene: NUP205 HGNC NCBI

Linked Data

dbSNP Id: rs570589241

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.135645085A>G , CM000669.2:g.135645085A>G GRCh38
NC_000007.13:g.135329833A>G , CM000669.1:g.135329833A>G GRCh37
NC_000007.12:g.134980373A>G NCBI36
NG_051184.1:g.92172A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000285968.11:c.5683+67A>G MANE Select ENSP00000285968.6:n.5683+67A>G
ENST00000285968.10:c.5683+67A>G ENSP00000285968.6:n.5683+67A>G
ENST00000461255.5:n.890+67A>G
ENST00000477620.5:c.1405+107A>G
ENST00000490439.1:c.120+67A>G
ENST00000607647.5:n.3961+67A>G
NM_015135.2:c.5683+67A>G NP_055950.1:n.5683+67A>G
XM_005250235.2:c.4609+67A>G XP_005250292.1:n.4609+67A>G
NM_001329434.1:c.4609+67A>G NP_001316363.1:n.4609+67A>G
NM_015135.3:c.5683+67A>G MANE Select NP_055950.2:n.5683+67A>G
NM_001329434.2:c.4609+67A>G NP_001316363.2:n.4609+67A>G