Canonical Allele Identifier: CA395993161

Gene: NUP93

Linked Data

• MyVariant Identifiers: chr16:g.56870582A>C (hg19) ; chr16:g.56836670A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56836670A>C , CM000678.2:g.56836670A>C	GRCh38
NC_000016.9:g.56870582A>C , CM000678.1:g.56870582A>C	GRCh37
NC_000016.8:g.55428083A>C	NCBI36
NG_052904.1:g.111566A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308159.10:c.1852A>C MANE Select	ENSP00000310668.5:p.Asn618His
ENST00000308159.9:c.1852A>C	ENSP00000310668.5:p.Asn618His
ENST00000542526.5:c.1483A>C	ENSP00000440235.1:p.Asn495His
ENST00000563405.1:c.46A>C	ENSP00000458078.1:p.Asn16His
ENST00000564887.5:c.1483A>C	ENSP00000458039.1:p.Asn495His
ENST00000569842.5:c.1852A>C	ENSP00000458101.1:p.Asn618His
NM_001242795.1:c.1483A>C	NP_001229724.1:p.Asn495His
NM_001242796.1:c.1483A>C	NP_001229725.1:p.Asn495His
NM_014669.4:c.1852A>C	NP_055484.3:p.Asn618His
XM_005256263.2:c.1852A>C	XP_005256320.1:p.Asn618His
NM_001242796.2:c.1483A>C	NP_001229725.1:p.Asn495His
XM_005256263.3:c.1852A>C	XP_005256320.1:p.Asn618His
NM_014669.5:c.1852A>C MANE Select	NP_055484.3:p.Asn618His
NM_001242795.2:c.1483A>C	NP_001229724.1:p.Asn495His