Canonical Allele Identifier: CA351901985

Gene: NGLY1

Linked Data

• MyVariant Identifiers: chr3:g.25778872C>G (hg19) ; chr3:g.25737381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25737381C>G , CM000665.2:g.25737381C>G	GRCh38
NC_000003.11:g.25778872C>G , CM000665.1:g.25778872C>G	GRCh37
NC_000003.10:g.25753876C>G	NCBI36
NG_034108.1:g.57659G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280700.10:c.956G>C MANE Select	ENSP00000280700.5:p.Cys319Ser
ENST00000463611.2:c.*1047G>C	ENSP00000501918.1:n.*1047G>C
ENST00000674841.1:n.1079G>C
ENST00000675178.1:n.168-3399G>C
ENST00000675217.1:c.*329G>C	ENSP00000502195.1:n.*329G>C
ENST00000675234.1:c.*453G>C	ENSP00000502740.1:n.*453G>C
ENST00000675680.1:c.391-981G>C
ENST00000676225.1:c.882-981G>C	ENSP00000501622.1:n.882-981G>C
ENST00000280699.13:c.707G>C
ENST00000280700.9:c.956G>C	ENSP00000280700.5:p.Cys319Ser
ENST00000308710.9:c.947G>C	ENSP00000307980.5:p.Cys316Ser
ENST00000396649.7:c.956G>C	ENSP00000379886.3:p.Cys319Ser
ENST00000417874.6:c.830G>C	ENSP00000389888.2:p.Cys277Ser
ENST00000428257.5:c.956G>C	ENSP00000387430.1:p.Cys319Ser
ENST00000493324.5:n.980G>C
NM_001145293.1:c.956G>C	NP_001138765.1:p.Cys319Ser
NM_001145294.1:c.830G>C	NP_001138766.1:p.Cys277Ser
NM_001145295.1:c.956G>C	NP_001138767.1:p.Cys319Ser
NM_018297.3:c.956G>C	NP_060767.2:p.Cys319Ser
XM_005265316.1:c.956G>C	XP_005265373.1:p.Cys319Ser
XM_005265317.1:c.956G>C	XP_005265374.1:p.Cys319Ser
XM_011533944.1:c.725G>C	XP_011532246.1:p.Cys242Ser
XM_011533945.1:c.956G>C	XP_011532247.1:p.Cys319Ser
XR_940470.1:n.1009G>C
XR_940471.1:n.1009G>C
XM_017006839.2:c.956G>C	XP_016862328.1:p.Cys319Ser
XR_001740200.2:n.1009G>C
XR_002959548.1:n.1009G>C
XR_940471.2:n.1009G>C
NM_018297.4:c.956G>C MANE Select	NP_060767.2:p.Cys319Ser
NM_001145293.2:c.956G>C	NP_001138765.1:p.Cys319Ser
NM_001145294.2:c.830G>C	NP_001138766.1:p.Cys277Ser
NM_001145295.2:c.956G>C	NP_001138767.1:p.Cys319Ser