Canonical Allele Identifier: CA2224333865

Gene: NUP93

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56836803T= , CM000678.2:g.56836803T=	GRCh38
NC_000016.9:g.56870715T= , CM000678.1:g.56870715T=	GRCh37
NC_000016.8:g.55428216T=	NCBI36
NG_052904.1:g.111699T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308159.10:c.1899+86T= MANE Select	ENSP00000310668.5:n.1899+86T=
ENST00000308159.9:c.1899+86T=	ENSP00000310668.5:n.1899+86T=
ENST00000542526.5:c.1530+86T=	ENSP00000440235.1:n.1530+86T=
ENST00000563405.1:c.93+86T=	ENSP00000458078.1:n.93+86T=
ENST00000564887.5:c.1530+86T=	ENSP00000458039.1:n.1530+86T=
ENST00000569842.5:c.1899+86T=	ENSP00000458101.1:n.1899+86T=
NM_001242795.1:c.1530+86T=	NP_001229724.1:n.1530+86T=
NM_001242796.1:c.1530+86T=	NP_001229725.1:n.1530+86T=
NM_014669.4:c.1899+86T=	NP_055484.3:n.1899+86T=
XM_005256263.2:c.1899+86T=	XP_005256320.1:n.1899+86T=
NM_001242796.2:c.1530+86T=	NP_001229725.1:n.1530+86T=
XM_005256263.3:c.1899+86T=	XP_005256320.1:n.1899+86T=
NM_014669.5:c.1899+86T= MANE Select	NP_055484.3:n.1899+86T=
NM_001242795.2:c.1530+86T=	NP_001229724.1:n.1530+86T=