Canonical Allele Identifier: CA351904711

Gene: NGLY1

Linked Data

• ClinVar Variation Id: 1704292
• ClinVar RCV Id: RCV002281639
• MyVariant Identifiers: chr3:g.25781291C>T (hg19) ; chr3:g.25739800C>T (hg38)
• MutSpliceDB: CA351904711

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25739800C>T , CM000665.2:g.25739800C>T	GRCh38
NC_000003.11:g.25781291C>T , CM000665.1:g.25781291C>T	GRCh37
NC_000003.10:g.25756295C>T	NCBI36
NG_034108.1:g.55240G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280700.10:c.659-1G>A MANE Select	ENSP00000280700.5:n.659-1G>A
ENST00000463611.2:c.*750-1G>A	ENSP00000501918.1:n.*750-1G>A
ENST00000674841.1:n.782-1G>A
ENST00000675178.1:n.168-5818G>A
ENST00000675217.1:c.*32-1G>A	ENSP00000502195.1:n.*32-1G>A
ENST00000675234.1:c.*156-1G>A	ENSP00000502740.1:n.*156-1G>A
ENST00000675680.1:c.168-1G>A
ENST00000676225.1:c.659-1G>A	ENSP00000501622.1:n.659-1G>A
ENST00000280699.13:c.633-2345G>A
ENST00000280700.9:c.659-1G>A	ENSP00000280700.5:n.659-1G>A
ENST00000308710.9:c.650-1G>A	ENSP00000307980.5:n.650-1G>A
ENST00000396649.7:c.659-1G>A	ENSP00000379886.3:n.659-1G>A
ENST00000417874.6:c.533-1G>A	ENSP00000389888.2:n.533-1G>A
ENST00000428257.5:c.659-1G>A	ENSP00000387430.1:n.659-1G>A
ENST00000493324.5:n.683-1G>A
NM_001145293.1:c.659-1G>A	NP_001138765.1:n.659-1G>A
NM_001145294.1:c.533-1G>A	NP_001138766.1:n.533-1G>A
NM_001145295.1:c.659-1G>A	NP_001138767.1:n.659-1G>A
NM_018297.3:c.659-1G>A	NP_060767.2:n.659-1G>A
XM_005265316.1:c.659-1G>A	XP_005265373.1:n.659-1G>A
XM_005265317.1:c.659-1G>A	XP_005265374.1:n.659-1G>A
XM_011533944.1:c.428-1G>A	XP_011532246.1:n.428-1G>A
XM_011533945.1:c.659-1G>A	XP_011532247.1:n.659-1G>A
XR_940470.1:n.712-1G>A
XR_940471.1:n.712-1G>A
XM_017006839.2:c.659-1G>A	XP_016862328.1:n.659-1G>A
XR_001740200.2:n.712-1G>A
XR_002959548.1:n.712-1G>A
XR_940471.2:n.712-1G>A
NM_018297.4:c.659-1G>A MANE Select	NP_060767.2:n.659-1G>A
NM_001145293.2:c.659-1G>A	NP_001138765.1:n.659-1G>A
NM_001145294.2:c.533-1G>A	NP_001138766.1:n.533-1G>A
NM_001145295.2:c.659-1G>A	NP_001138767.1:n.659-1G>A