Canonical Allele Identifier: CA622339538

Gene: NUP93

Linked Data

• dbSNP Id: rs1255740194
• gnomAD v2: 16-56870650-T-C
• gnomAD v3: 16-56836738-T-C
• gnomAD v4: 16-56836738-T-C
• MyVariant Identifiers: chr16:g.56870650T>C (hg19) ; chr16:g.56836738T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56836738T>C , CM000678.2:g.56836738T>C	GRCh38
NC_000016.9:g.56870650T>C , CM000678.1:g.56870650T>C	GRCh37
NC_000016.8:g.55428151T>C	NCBI36
NG_052904.1:g.111634T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308159.10:c.1899+21T>C MANE Select	ENSP00000310668.5:n.1899+21T>C
ENST00000308159.9:c.1899+21T>C	ENSP00000310668.5:n.1899+21T>C
ENST00000542526.5:c.1530+21T>C	ENSP00000440235.1:n.1530+21T>C
ENST00000563405.1:c.93+21T>C	ENSP00000458078.1:n.93+21T>C
ENST00000564887.5:c.1530+21T>C	ENSP00000458039.1:n.1530+21T>C
ENST00000569842.5:c.1899+21T>C	ENSP00000458101.1:n.1899+21T>C
NM_001242795.1:c.1530+21T>C	NP_001229724.1:n.1530+21T>C
NM_001242796.1:c.1530+21T>C	NP_001229725.1:n.1530+21T>C
NM_014669.4:c.1899+21T>C	NP_055484.3:n.1899+21T>C
XM_005256263.2:c.1899+21T>C	XP_005256320.1:n.1899+21T>C
NM_001242796.2:c.1530+21T>C	NP_001229725.1:n.1530+21T>C
XM_005256263.3:c.1899+21T>C	XP_005256320.1:n.1899+21T>C
NM_014669.5:c.1899+21T>C MANE Select	NP_055484.3:n.1899+21T>C
NM_001242795.2:c.1530+21T>C	NP_001229724.1:n.1530+21T>C