Canonical Allele Identifier: CA1352483311
Gene: NGLY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.25737366C= , CM000665.2:g.25737366C= GRCh38
NC_000003.11:g.25778857C= , CM000665.1:g.25778857C= GRCh37
NC_000003.10:g.25753861C= NCBI36
NG_034108.1:g.57674G=

Transcript Alleles

HGVS Amino-acid change
ENST00000280700.10:c.971G= MANE Select ENSP00000280700.5:p.Gly324=
ENST00000463611.2:c.*1062G= ENSP00000501918.1:n.*1062G=
ENST00000674841.1:n.1094G=
ENST00000675178.1:n.168-3384G=
ENST00000675217.1:c.*344G= ENSP00000502195.1:n.*344G=
ENST00000675234.1:c.*468G= ENSP00000502740.1:n.*468G=
ENST00000675680.1:c.391-966G=
ENST00000676225.1:c.882-966G= ENSP00000501622.1:n.882-966G=
ENST00000280699.13:c.722G=
ENST00000280700.9:c.971G= ENSP00000280700.5:p.Gly324=
ENST00000308710.9:c.962G= ENSP00000307980.5:p.Gly321=
ENST00000396649.7:c.971G= ENSP00000379886.3:p.Gly324=
ENST00000417874.6:c.845G= ENSP00000389888.2:p.Gly282=
ENST00000428257.5:c.971G= ENSP00000387430.1:p.Gly324=
ENST00000493324.5:n.995G=
NM_001145293.1:c.971G= NP_001138765.1:p.Gly324=
NM_001145294.1:c.845G= NP_001138766.1:p.Gly282=
NM_001145295.1:c.971G= NP_001138767.1:p.Gly324=
NM_018297.3:c.971G= NP_060767.2:p.Gly324=
XM_005265316.1:c.971G= XP_005265373.1:p.Gly324=
XM_005265317.1:c.971G= XP_005265374.1:p.Gly324=
XM_011533944.1:c.740G= XP_011532246.1:p.Gly247=
XM_011533945.1:c.971G= XP_011532247.1:p.Gly324=
XR_940470.1:n.1024G=
XR_940471.1:n.1024G=
XM_017006839.2:c.971G= XP_016862328.1:p.Gly324=
XR_001740200.2:n.1024G=
XR_002959548.1:n.1024G=
XR_940471.2:n.1024G=
NM_018297.4:c.971G= MANE Select NP_060767.2:p.Gly324=
NM_001145293.2:c.971G= NP_001138765.1:p.Gly324=
NM_001145294.2:c.845G= NP_001138766.1:p.Gly282=
NM_001145295.2:c.971G= NP_001138767.1:p.Gly324=