Canonical Allele Identifier: CA495600418

Gene: NUP93

Linked Data

• MyVariant Identifiers: chr16:g.56867266G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56833354G>T , CM000678.2:g.56833354G>T	GRCh38
NC_000016.9:g.56867266G>T , CM000678.1:g.56867266G>T	GRCh37
NC_000016.8:g.55424767G>T	NCBI36
NG_052904.1:g.108250G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308159.10:c.1485G>T MANE Select	ENSP00000310668.5:p.Val495=
ENST00000308159.9:c.1485G>T	ENSP00000310668.5:p.Val495=
ENST00000542526.5:c.1116G>T	ENSP00000440235.1:p.Val372=
ENST00000563437.1:n.727G>T
ENST00000564887.5:c.1116G>T	ENSP00000458039.1:p.Val372=
ENST00000569842.5:c.1485G>T	ENSP00000458101.1:p.Val495=
NM_001242795.1:c.1116G>T	NP_001229724.1:p.Val372=
NM_001242796.1:c.1116G>T	NP_001229725.1:p.Val372=
NM_014669.4:c.1485G>T	NP_055484.3:p.Val495=
XM_005256263.2:c.1485G>T	XP_005256320.1:p.Val495=
NM_001242796.2:c.1116G>T	NP_001229725.1:p.Val372=
XM_005256263.3:c.1485G>T	XP_005256320.1:p.Val495=
NM_014669.5:c.1485G>T MANE Select	NP_055484.3:p.Val495=
NM_001242795.2:c.1116G>T	NP_001229724.1:p.Val372=