Canonical Allele Identifier: CA2224333800

Gene: NUP93

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56836638_56836641delinsCTAT , CM000678.2:g.56836638_56836641delinsCTAT	GRCh38
NC_000016.9:g.56870550_56870553delinsCTAT , CM000678.1:g.56870550_56870553delinsCTAT	GRCh37
NC_000016.8:g.55428051_55428054delinsCTAT	NCBI36
NG_052904.1:g.111534_111537delinsCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308159.10:c.1820_1823delinsCTAT MANE Select	ENSP00000310668.5:p.Pro607=
ENST00000308159.9:c.1820_1823delinsCTAT	ENSP00000310668.5:p.Pro607=
ENST00000542526.5:c.1451_1454delinsCTAT	ENSP00000440235.1:p.Pro484=
ENST00000563405.1:c.14_17delinsCTAT	ENSP00000458078.1:p.Pro5=
ENST00000564887.5:c.1451_1454delinsCTAT	ENSP00000458039.1:p.Pro484=
ENST00000569842.5:c.1820_1823delinsCTAT	ENSP00000458101.1:p.Pro607=
NM_001242795.1:c.1451_1454delinsCTAT	NP_001229724.1:p.Pro484=
NM_001242796.1:c.1451_1454delinsCTAT	NP_001229725.1:p.Pro484=
NM_014669.4:c.1820_1823delinsCTAT	NP_055484.3:p.Pro607=
XM_005256263.2:c.1820_1823delinsCTAT	XP_005256320.1:p.Pro607=
NM_001242796.2:c.1451_1454delinsCTAT	NP_001229725.1:p.Pro484=
XM_005256263.3:c.1820_1823delinsCTAT	XP_005256320.1:p.Pro607=
NM_014669.5:c.1820_1823delinsCTAT MANE Select	NP_055484.3:p.Pro607=
NM_001242795.2:c.1451_1454delinsCTAT	NP_001229724.1:p.Pro484=