Canonical Allele Identifier: CA1352483353

Gene: NGLY1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25737453T= , CM000665.2:g.25737453T=	GRCh38
NC_000003.11:g.25778944T= , CM000665.1:g.25778944T=	GRCh37
NC_000003.10:g.25753948T=	NCBI36
NG_034108.1:g.57587A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280700.10:c.884A= MANE Select	ENSP00000280700.5:p.Tyr295=
ENST00000463611.2:c.*975A=	ENSP00000501918.1:n.*975A=
ENST00000674841.1:n.1007A=
ENST00000675178.1:n.168-3471A=
ENST00000675217.1:c.*257A=	ENSP00000502195.1:n.*257A=
ENST00000675234.1:c.*381A=	ENSP00000502740.1:n.*381A=
ENST00000675680.1:c.391-1053A=
ENST00000676225.1:c.882-1053A=	ENSP00000501622.1:n.882-1053A=
ENST00000280699.13:c.635A=
ENST00000280700.9:c.884A=	ENSP00000280700.5:p.Tyr295=
ENST00000308710.9:c.875A=	ENSP00000307980.5:p.Tyr292=
ENST00000396649.7:c.884A=	ENSP00000379886.3:p.Tyr295=
ENST00000417874.6:c.758A=	ENSP00000389888.2:p.Tyr253=
ENST00000428257.5:c.884A=	ENSP00000387430.1:p.Tyr295=
ENST00000493324.5:n.908A=
NM_001145293.1:c.884A=	NP_001138765.1:p.Tyr295=
NM_001145294.1:c.758A=	NP_001138766.1:p.Tyr253=
NM_001145295.1:c.884A=	NP_001138767.1:p.Tyr295=
NM_018297.3:c.884A=	NP_060767.2:p.Tyr295=
XM_005265316.1:c.884A=	XP_005265373.1:p.Tyr295=
XM_005265317.1:c.884A=	XP_005265374.1:p.Tyr295=
XM_011533944.1:c.653A=	XP_011532246.1:p.Tyr218=
XM_011533945.1:c.884A=	XP_011532247.1:p.Tyr295=
XR_940470.1:n.937A=
XR_940471.1:n.937A=
XM_017006839.2:c.884A=	XP_016862328.1:p.Tyr295=
XR_001740200.2:n.937A=
XR_002959548.1:n.937A=
XR_940471.2:n.937A=
NM_018297.4:c.884A= MANE Select	NP_060767.2:p.Tyr295=
NM_001145293.2:c.884A=	NP_001138765.1:p.Tyr295=
NM_001145294.2:c.758A=	NP_001138766.1:p.Tyr253=
NM_001145295.2:c.884A=	NP_001138767.1:p.Tyr295=