Canonical Allele Identifier: CA351901897

Gene: NGLY1

Linked Data

• MyVariant Identifiers: chr3:g.25778854A>T (hg19) ; chr3:g.25737363A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25737363A>T , CM000665.2:g.25737363A>T	GRCh38
NC_000003.11:g.25778854A>T , CM000665.1:g.25778854A>T	GRCh37
NC_000003.10:g.25753858A>T	NCBI36
NG_034108.1:g.57677T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000280700.10:c.974T>A MANE Select	ENSP00000280700.5:p.Phe325Tyr
ENST00000463611.2:c.*1065T>A	ENSP00000501918.1:n.*1065T>A
ENST00000674841.1:n.1097T>A
ENST00000675178.1:n.168-3381T>A
ENST00000675217.1:c.*347T>A	ENSP00000502195.1:n.*347T>A
ENST00000675234.1:c.*471T>A	ENSP00000502740.1:n.*471T>A
ENST00000675680.1:c.391-963T>A
ENST00000676225.1:c.882-963T>A	ENSP00000501622.1:n.882-963T>A
ENST00000280699.13:c.725T>A
ENST00000280700.9:c.974T>A	ENSP00000280700.5:p.Phe325Tyr
ENST00000308710.9:c.965T>A	ENSP00000307980.5:p.Phe322Tyr
ENST00000396649.7:c.974T>A	ENSP00000379886.3:p.Phe325Tyr
ENST00000417874.6:c.848T>A	ENSP00000389888.2:p.Phe283Tyr
ENST00000428257.5:c.974T>A	ENSP00000387430.1:p.Phe325Tyr
ENST00000493324.5:n.998T>A
NM_001145293.1:c.974T>A	NP_001138765.1:p.Phe325Tyr
NM_001145294.1:c.848T>A	NP_001138766.1:p.Phe283Tyr
NM_001145295.1:c.974T>A	NP_001138767.1:p.Phe325Tyr
NM_018297.3:c.974T>A	NP_060767.2:p.Phe325Tyr
XM_005265316.1:c.974T>A	XP_005265373.1:p.Phe325Tyr
XM_005265317.1:c.974T>A	XP_005265374.1:p.Phe325Tyr
XM_011533944.1:c.743T>A	XP_011532246.1:p.Phe248Tyr
XM_011533945.1:c.974T>A	XP_011532247.1:p.Phe325Tyr
XR_940470.1:n.1027T>A
XR_940471.1:n.1027T>A
XM_017006839.2:c.974T>A	XP_016862328.1:p.Phe325Tyr
XR_001740200.2:n.1027T>A
XR_002959548.1:n.1027T>A
XR_940471.2:n.1027T>A
NM_018297.4:c.974T>A MANE Select	NP_060767.2:p.Phe325Tyr
NM_001145293.2:c.974T>A	NP_001138765.1:p.Phe325Tyr
NM_001145294.2:c.848T>A	NP_001138766.1:p.Phe283Tyr
NM_001145295.2:c.974T>A	NP_001138767.1:p.Phe325Tyr