Canonical Allele Identifier: CA2224332234

Gene: NUP93

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56833314T= , CM000678.2:g.56833314T=	GRCh38
NC_000016.9:g.56867226T= , CM000678.1:g.56867226T=	GRCh37
NC_000016.8:g.55424727T=	NCBI36
NG_052904.1:g.108210T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000308159.10:c.1445T= MANE Select	ENSP00000310668.5:p.Met482=
ENST00000308159.9:c.1445T=	ENSP00000310668.5:p.Met482=
ENST00000542526.5:c.1076T=	ENSP00000440235.1:p.Met359=
ENST00000563437.1:n.687T=
ENST00000564887.5:c.1076T=	ENSP00000458039.1:p.Met359=
ENST00000569842.5:c.1445T=	ENSP00000458101.1:p.Met482=
NM_001242795.1:c.1076T=	NP_001229724.1:p.Met359=
NM_001242796.1:c.1076T=	NP_001229725.1:p.Met359=
NM_014669.4:c.1445T=	NP_055484.3:p.Met482=
XM_005256263.2:c.1445T=	XP_005256320.1:p.Met482=
NM_001242796.2:c.1076T=	NP_001229725.1:p.Met359=
XM_005256263.3:c.1445T=	XP_005256320.1:p.Met482=
NM_014669.5:c.1445T= MANE Select	NP_055484.3:p.Met482=
NM_001242795.2:c.1076T=	NP_001229724.1:p.Met359=