Canonical Allele Identifier: CA2830544139

Gene: NUP205

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.135645050_135645051insTTCATAAA , CM000669.2:g.135645050_135645051insTTCATAAA	GRCh38
NC_000007.13:g.135329798_135329799insTTCATAAA , CM000669.1:g.135329798_135329799insTTCATAAA	GRCh37
NC_000007.12:g.134980338_134980339insTTCATAAA	NCBI36
NG_051184.1:g.92137_92138insTTCATAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285968.11:c.5683+32_5683+33insTTCATAAA MANE Select	ENSP00000285968.6:n.5683+32_5683+33insTTCATAAA
ENST00000285968.10:c.5683+32_5683+33insTTCATAAA	ENSP00000285968.6:n.5683+32_5683+33insTTCATAAA
ENST00000461255.5:n.890+32_890+33insTTCATAAA
ENST00000477620.5:c.1405+72_1405+73insTTCATAAA
ENST00000490439.1:c.120+32_120+33insTTCATAAA
ENST00000607647.5:n.3961+32_3961+33insTTCATAAA
NM_015135.2:c.5683+32_5683+33insTTCATAAA	NP_055950.1:n.5683+32_5683+33insTTCATAAA
XM_005250235.2:c.4609+32_4609+33insTTCATAAA	XP_005250292.1:n.4609+32_4609+33insTTCATAAA
NM_001329434.1:c.4609+32_4609+33insTTCATAAA	NP_001316363.1:n.4609+32_4609+33insTTCATAAA
NM_015135.3:c.5683+32_5683+33insTTCATAAA MANE Select	NP_055950.2:n.5683+32_5683+33insTTCATAAA
NM_001329434.2:c.4609+32_4609+33insTTCATAAA	NP_001316363.2:n.4609+32_4609+33insTTCATAAA