Canonical Allele Identifier: CA1352483359

Gene: NGLY1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25737462T= , CM000665.2:g.25737462T=	GRCh38
NC_000003.11:g.25778953T= , CM000665.1:g.25778953T=	GRCh37
NC_000003.10:g.25753957T=	NCBI36
NG_034108.1:g.57578A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280700.10:c.882-7A= MANE Select	ENSP00000280700.5:n.882-7A=
ENST00000463611.2:c.*973-7A=	ENSP00000501918.1:n.*973-7A=
ENST00000674841.1:n.1005-7A=
ENST00000675178.1:n.168-3480A=
ENST00000675217.1:c.*255-7A=	ENSP00000502195.1:n.*255-7A=
ENST00000675234.1:c.*379-7A=	ENSP00000502740.1:n.*379-7A=
ENST00000675680.1:c.391-1062A=
ENST00000676225.1:c.882-1062A=	ENSP00000501622.1:n.882-1062A=
ENST00000280699.13:c.633-7A=
ENST00000280700.9:c.882-7A=	ENSP00000280700.5:n.882-7A=
ENST00000308710.9:c.873-7A=	ENSP00000307980.5:n.873-7A=
ENST00000396649.7:c.882-7A=	ENSP00000379886.3:n.882-7A=
ENST00000417874.6:c.756-7A=	ENSP00000389888.2:n.756-7A=
ENST00000428257.5:c.882-7A=	ENSP00000387430.1:n.882-7A=
ENST00000493324.5:n.906-7A=
NM_001145293.1:c.882-7A=	NP_001138765.1:n.882-7A=
NM_001145294.1:c.756-7A=	NP_001138766.1:n.756-7A=
NM_001145295.1:c.882-7A=	NP_001138767.1:n.882-7A=
NM_018297.3:c.882-7A=	NP_060767.2:n.882-7A=
XM_005265316.1:c.882-7A=	XP_005265373.1:n.882-7A=
XM_005265317.1:c.882-7A=	XP_005265374.1:n.882-7A=
XM_011533944.1:c.651-7A=	XP_011532246.1:n.651-7A=
XM_011533945.1:c.882-7A=	XP_011532247.1:n.882-7A=
XR_940470.1:n.935-7A=
XR_940471.1:n.935-7A=
XM_017006839.2:c.882-7A=	XP_016862328.1:n.882-7A=
XR_001740200.2:n.935-7A=
XR_002959548.1:n.935-7A=
XR_940471.2:n.935-7A=
NM_018297.4:c.882-7A= MANE Select	NP_060767.2:n.882-7A=
NM_001145293.2:c.882-7A=	NP_001138765.1:n.882-7A=
NM_001145294.2:c.756-7A=	NP_001138766.1:n.756-7A=
NM_001145295.2:c.882-7A=	NP_001138767.1:n.882-7A=