Canonical Allele Identifier: CA432843147

Gene: NGLY1

Linked Data

• MyVariant Identifiers: chr3:g.25778862A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25737371A>T , CM000665.2:g.25737371A>T	GRCh38
NC_000003.11:g.25778862A>T , CM000665.1:g.25778862A>T	GRCh37
NC_000003.10:g.25753866A>T	NCBI36
NG_034108.1:g.57669T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280700.10:c.966T>A MANE Select	ENSP00000280700.5:p.Ala322=
ENST00000463611.2:c.*1057T>A	ENSP00000501918.1:n.*1057T>A
ENST00000674841.1:n.1089T>A
ENST00000675178.1:n.168-3389T>A
ENST00000675217.1:c.*339T>A	ENSP00000502195.1:n.*339T>A
ENST00000675234.1:c.*463T>A	ENSP00000502740.1:n.*463T>A
ENST00000675680.1:c.391-971T>A
ENST00000676225.1:c.882-971T>A	ENSP00000501622.1:n.882-971T>A
ENST00000280699.13:c.717T>A
ENST00000280700.9:c.966T>A	ENSP00000280700.5:p.Ala322=
ENST00000308710.9:c.957T>A	ENSP00000307980.5:p.Ala319=
ENST00000396649.7:c.966T>A	ENSP00000379886.3:p.Ala322=
ENST00000417874.6:c.840T>A	ENSP00000389888.2:p.Ala280=
ENST00000428257.5:c.966T>A	ENSP00000387430.1:p.Ala322=
ENST00000493324.5:n.990T>A
NM_001145293.1:c.966T>A	NP_001138765.1:p.Ala322=
NM_001145294.1:c.840T>A	NP_001138766.1:p.Ala280=
NM_001145295.1:c.966T>A	NP_001138767.1:p.Ala322=
NM_018297.3:c.966T>A	NP_060767.2:p.Ala322=
XM_005265316.1:c.966T>A	XP_005265373.1:p.Ala322=
XM_005265317.1:c.966T>A	XP_005265374.1:p.Ala322=
XM_011533944.1:c.735T>A	XP_011532246.1:p.Ala245=
XM_011533945.1:c.966T>A	XP_011532247.1:p.Ala322=
XR_940470.1:n.1019T>A
XR_940471.1:n.1019T>A
XM_017006839.2:c.966T>A	XP_016862328.1:p.Ala322=
XR_001740200.2:n.1019T>A
XR_002959548.1:n.1019T>A
XR_940471.2:n.1019T>A
NM_018297.4:c.966T>A MANE Select	NP_060767.2:p.Ala322=
NM_001145293.2:c.966T>A	NP_001138765.1:p.Ala322=
NM_001145294.2:c.840T>A	NP_001138766.1:p.Ala280=
NM_001145295.2:c.966T>A	NP_001138767.1:p.Ala322=