Canonical Allele Identifier: CA432843143

Gene: NGLY1

Linked Data

• MyVariant Identifiers: chr3:g.25778859T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25737368T>A , CM000665.2:g.25737368T>A	GRCh38
NC_000003.11:g.25778859T>A , CM000665.1:g.25778859T>A	GRCh37
NC_000003.10:g.25753863T>A	NCBI36
NG_034108.1:g.57672A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000280700.10:c.969A>T MANE Select	ENSP00000280700.5:p.Val323=
ENST00000463611.2:c.*1060A>T	ENSP00000501918.1:n.*1060A>T
ENST00000674841.1:n.1092A>T
ENST00000675178.1:n.168-3386A>T
ENST00000675217.1:c.*342A>T	ENSP00000502195.1:n.*342A>T
ENST00000675234.1:c.*466A>T	ENSP00000502740.1:n.*466A>T
ENST00000675680.1:c.391-968A>T
ENST00000676225.1:c.882-968A>T	ENSP00000501622.1:n.882-968A>T
ENST00000280699.13:c.720A>T
ENST00000280700.9:c.969A>T	ENSP00000280700.5:p.Val323=
ENST00000308710.9:c.960A>T	ENSP00000307980.5:p.Val320=
ENST00000396649.7:c.969A>T	ENSP00000379886.3:p.Val323=
ENST00000417874.6:c.843A>T	ENSP00000389888.2:p.Val281=
ENST00000428257.5:c.969A>T	ENSP00000387430.1:p.Val323=
ENST00000493324.5:n.993A>T
NM_001145293.1:c.969A>T	NP_001138765.1:p.Val323=
NM_001145294.1:c.843A>T	NP_001138766.1:p.Val281=
NM_001145295.1:c.969A>T	NP_001138767.1:p.Val323=
NM_018297.3:c.969A>T	NP_060767.2:p.Val323=
XM_005265316.1:c.969A>T	XP_005265373.1:p.Val323=
XM_005265317.1:c.969A>T	XP_005265374.1:p.Val323=
XM_011533944.1:c.738A>T	XP_011532246.1:p.Val246=
XM_011533945.1:c.969A>T	XP_011532247.1:p.Val323=
XR_940470.1:n.1022A>T
XR_940471.1:n.1022A>T
XM_017006839.2:c.969A>T	XP_016862328.1:p.Val323=
XR_001740200.2:n.1022A>T
XR_002959548.1:n.1022A>T
XR_940471.2:n.1022A>T
NM_018297.4:c.969A>T MANE Select	NP_060767.2:p.Val323=
NM_001145293.2:c.969A>T	NP_001138765.1:p.Val323=
NM_001145294.2:c.843A>T	NP_001138766.1:p.Val281=
NM_001145295.2:c.969A>T	NP_001138767.1:p.Val323=