Canonical Allele Identifier: CA2537768202
Gene: NGLY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.25737394_25737395insGTAATAATACCAACCTTCCAGGTTTTTTGAAGGG , CM000665.2:g.25737394_25737395insGTAATAATACCAACCTTCCAGGTTTTTTGAAGGG GRCh38
NC_000003.11:g.25778885_25778886insGTAATAATACCAACCTTCCAGGTTTTTTGAAGGG , CM000665.1:g.25778885_25778886insGTAATAATACCAACCTTCCAGGTTTTTTGAAGGG GRCh37
NC_000003.10:g.25753889_25753890insGTAATAATACCAACCTTCCAGGTTTTTTGAAGGG NCBI36
NG_034108.1:g.57645_57646insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000280700.10:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC MANE Select ENSP00000280700.5:p.Cys315ProfsTer23
ENST00000463611.2:c.*1033_*1034insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000501918.1:n.*1033_*1034insCCCTTCAAAAAACCTGGAAGGTTGGTA...
ENST00000674841.1:n.1065_1066insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
ENST00000675178.1:n.168-3413_168-3412insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
ENST00000675217.1:c.*315_*316insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000502195.1:n.*315_*316insCCCTTCAAAAAACCTGGAAGGTTGGTATT...
ENST00000675234.1:c.*439_*440insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000502740.1:n.*439_*440insCCCTTCAAAAAACCTGGAAGGTTGGTATT...
ENST00000675680.1:c.391-995_391-994insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
ENST00000676225.1:c.882-995_882-994insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000501622.1:n.882-995_882-994insCCCTTCAAAAAACCTGGAAGGTT...
ENST00000280699.13:c.693_694insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
ENST00000280700.9:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000280700.5:p.Cys315ProfsTer23
ENST00000308710.9:c.933_934insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000307980.5:p.Cys312ProfsTer23
ENST00000396649.7:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000379886.3:p.Cys315ProfsTer23
ENST00000417874.6:c.816_817insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000389888.2:p.Cys273ProfsTer23
ENST00000428257.5:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC ENSP00000387430.1:p.Cys315ProfsTer23
ENST00000493324.5:n.966_967insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
NM_001145293.1:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC NP_001138765.1:p.Cys315ProfsTer23
NM_001145294.1:c.816_817insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC NP_001138766.1:p.Cys273ProfsTer23
NM_001145295.1:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC NP_001138767.1:p.Cys315ProfsTer23
NM_018297.3:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC NP_060767.2:p.Cys315ProfsTer23
XM_005265316.1:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC XP_005265373.1:p.Cys315ProfsTer23
XM_005265317.1:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC XP_005265374.1:p.Cys315ProfsTer23
XM_011533944.1:c.711_712insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC XP_011532246.1:p.Cys238ProfsTer23
XM_011533945.1:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC XP_011532247.1:p.Cys315ProfsTer23
XR_940470.1:n.995_996insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
XR_940471.1:n.995_996insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
XM_017006839.2:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC XP_016862328.1:p.Cys315ProfsTer23
XR_001740200.2:n.995_996insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
XR_002959548.1:n.995_996insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
XR_940471.2:n.995_996insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC
NM_018297.4:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC MANE Select NP_060767.2:p.Cys315ProfsTer23
NM_001145293.2:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC NP_001138765.1:p.Cys315ProfsTer23
NM_001145294.2:c.816_817insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC NP_001138766.1:p.Cys273ProfsTer23
NM_001145295.2:c.942_943insCCCTTCAAAAAACCTGGAAGGTTGGTATTATTAC NP_001138767.1:p.Cys315ProfsTer23