Canonical Allele Identifier: CA2838283415
Gene: NUP205 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.135584797dup , CM000669.2:g.135584797dup GRCh38
NC_000007.13:g.135269545dup , CM000669.1:g.135269545dup GRCh37
NC_000007.12:g.134920085dup NCBI36
NG_051184.1:g.31884dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000285968.11:c.1043-35dup MANE Select ENSP00000285968.6:n.1043-35dup
ENST00000285968.10:c.1043-35dup ENSP00000285968.6:n.1043-35dup
NM_015135.2:c.1043-35dup NP_055950.1:n.1043-35dup
XM_005250235.2:c.-32-35dup XP_005250292.1:n.-32-35dup
NM_001329434.1:c.-32-35dup NP_001316363.1:n.-32-35dup
NM_015135.3:c.1043-35dup MANE Select NP_055950.2:n.1043-35dup
NM_001329434.2:c.-32-35dup NP_001316363.2:n.-32-35dup