Canonical Allele Identifier: CA351902214

Gene: NGLY1

Linked Data

• MyVariant Identifiers: chr3:g.25778920T>A (hg19) ; chr3:g.25737429T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25737429T>A , CM000665.2:g.25737429T>A	GRCh38
NC_000003.11:g.25778920T>A , CM000665.1:g.25778920T>A	GRCh37
NC_000003.10:g.25753924T>A	NCBI36
NG_034108.1:g.57611A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280700.10:c.908A>T MANE Select	ENSP00000280700.5:p.Glu303Val
ENST00000463611.2:c.*999A>T	ENSP00000501918.1:n.*999A>T
ENST00000674841.1:n.1031A>T
ENST00000675178.1:n.168-3447A>T
ENST00000675217.1:c.*281A>T	ENSP00000502195.1:n.*281A>T
ENST00000675234.1:c.*405A>T	ENSP00000502740.1:n.*405A>T
ENST00000675680.1:c.391-1029A>T
ENST00000676225.1:c.882-1029A>T	ENSP00000501622.1:n.882-1029A>T
ENST00000280699.13:c.659A>T
ENST00000280700.9:c.908A>T	ENSP00000280700.5:p.Glu303Val
ENST00000308710.9:c.899A>T	ENSP00000307980.5:p.Glu300Val
ENST00000396649.7:c.908A>T	ENSP00000379886.3:p.Glu303Val
ENST00000417874.6:c.782A>T	ENSP00000389888.2:p.Glu261Val
ENST00000428257.5:c.908A>T	ENSP00000387430.1:p.Glu303Val
ENST00000493324.5:n.932A>T
NM_001145293.1:c.908A>T	NP_001138765.1:p.Glu303Val
NM_001145294.1:c.782A>T	NP_001138766.1:p.Glu261Val
NM_001145295.1:c.908A>T	NP_001138767.1:p.Glu303Val
NM_018297.3:c.908A>T	NP_060767.2:p.Glu303Val
XM_005265316.1:c.908A>T	XP_005265373.1:p.Glu303Val
XM_005265317.1:c.908A>T	XP_005265374.1:p.Glu303Val
XM_011533944.1:c.677A>T	XP_011532246.1:p.Glu226Val
XM_011533945.1:c.908A>T	XP_011532247.1:p.Glu303Val
XR_940470.1:n.961A>T
XR_940471.1:n.961A>T
XM_017006839.2:c.908A>T	XP_016862328.1:p.Glu303Val
XR_001740200.2:n.961A>T
XR_002959548.1:n.961A>T
XR_940471.2:n.961A>T
NM_018297.4:c.908A>T MANE Select	NP_060767.2:p.Glu303Val
NM_001145293.2:c.908A>T	NP_001138765.1:p.Glu303Val
NM_001145294.2:c.782A>T	NP_001138766.1:p.Glu261Val
NM_001145295.2:c.908A>T	NP_001138767.1:p.Glu303Val