Canonical Allele Identifier: CA2224333821

Gene: NUP93

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56836706G= , CM000678.2:g.56836706G=	GRCh38
NC_000016.9:g.56870618G= , CM000678.1:g.56870618G=	GRCh37
NC_000016.8:g.55428119G=	NCBI36
NG_052904.1:g.111602G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308159.10:c.1888G= MANE Select	ENSP00000310668.5:p.Asp630=
ENST00000308159.9:c.1888G=	ENSP00000310668.5:p.Asp630=
ENST00000542526.5:c.1519G=	ENSP00000440235.1:p.Asp507=
ENST00000563405.1:c.82G=	ENSP00000458078.1:p.Asp28=
ENST00000564887.5:c.1519G=	ENSP00000458039.1:p.Asp507=
ENST00000569842.5:c.1888G=	ENSP00000458101.1:p.Asp630=
NM_001242795.1:c.1519G=	NP_001229724.1:p.Asp507=
NM_001242796.1:c.1519G=	NP_001229725.1:p.Asp507=
NM_014669.4:c.1888G=	NP_055484.3:p.Asp630=
XM_005256263.2:c.1888G=	XP_005256320.1:p.Asp630=
NM_001242796.2:c.1519G=	NP_001229725.1:p.Asp507=
XM_005256263.3:c.1888G=	XP_005256320.1:p.Asp630=
NM_014669.5:c.1888G= MANE Select	NP_055484.3:p.Asp630=
NM_001242795.2:c.1519G=	NP_001229724.1:p.Asp507=