Canonical Allele Identifier: CA2807158976

Gene: NUP93

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56836740_56836741insCGCC , CM000678.2:g.56836740_56836741insCGCC	GRCh38
NC_000016.9:g.56870652_56870653insCGCC , CM000678.1:g.56870652_56870653insCGCC	GRCh37
NC_000016.8:g.55428153_55428154insCGCC	NCBI36
NG_052904.1:g.111636_111637insCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308159.10:c.1899+23_1899+24insCGCC MANE Select	ENSP00000310668.5:n.1899+23_1899+24insCGCC
ENST00000308159.9:c.1899+23_1899+24insCGCC	ENSP00000310668.5:n.1899+23_1899+24insCGCC
ENST00000542526.5:c.1530+23_1530+24insCGCC	ENSP00000440235.1:n.1530+23_1530+24insCGCC
ENST00000563405.1:c.93+23_93+24insCGCC	ENSP00000458078.1:n.93+23_93+24insCGCC
ENST00000564887.5:c.1530+23_1530+24insCGCC	ENSP00000458039.1:n.1530+23_1530+24insCGCC
ENST00000569842.5:c.1899+23_1899+24insCGCC	ENSP00000458101.1:n.1899+23_1899+24insCGCC
NM_001242795.1:c.1530+23_1530+24insCGCC	NP_001229724.1:n.1530+23_1530+24insCGCC
NM_001242796.1:c.1530+23_1530+24insCGCC	NP_001229725.1:n.1530+23_1530+24insCGCC
NM_014669.4:c.1899+23_1899+24insCGCC	NP_055484.3:n.1899+23_1899+24insCGCC
XM_005256263.2:c.1899+23_1899+24insCGCC	XP_005256320.1:n.1899+23_1899+24insCGCC
NM_001242796.2:c.1530+23_1530+24insCGCC	NP_001229725.1:n.1530+23_1530+24insCGCC
XM_005256263.3:c.1899+23_1899+24insCGCC	XP_005256320.1:n.1899+23_1899+24insCGCC
NM_014669.5:c.1899+23_1899+24insCGCC MANE Select	NP_055484.3:n.1899+23_1899+24insCGCC
NM_001242795.2:c.1530+23_1530+24insCGCC	NP_001229724.1:n.1530+23_1530+24insCGCC