Canonical Allele Identifier: CA2580754219

Gene: NUP205

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.135645230T= , CM000669.2:g.135645230T=	GRCh38
NC_000007.13:g.135329978T= , CM000669.1:g.135329978T=	GRCh37
NC_000007.12:g.134980518T=	NCBI36
NG_051184.1:g.92317T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285968.11:c.5683+212T= MANE Select	ENSP00000285968.6:n.5683+212T=
ENST00000285968.10:c.5683+212T=	ENSP00000285968.6:n.5683+212T=
ENST00000461255.5:n.890+212T=
ENST00000477620.5:c.1405+252T=
ENST00000490439.1:c.120+212T=
ENST00000607647.5:n.3961+212T=
NM_015135.2:c.5683+212T=	NP_055950.1:n.5683+212T=
XM_005250235.2:c.4609+212T=	XP_005250292.1:n.4609+212T=
NM_001329434.1:c.4609+212T=	NP_001316363.1:n.4609+212T=
NM_015135.3:c.5683+212T= MANE Select	NP_055950.2:n.5683+212T=
NM_001329434.2:c.4609+212T=	NP_001316363.2:n.4609+212T=