Canonical Allele Identifier: CA432843142

Gene: NGLY1

Linked Data

• MyVariant Identifiers: chr3:g.25778856C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25737365C>G , CM000665.2:g.25737365C>G	GRCh38
NC_000003.11:g.25778856C>G , CM000665.1:g.25778856C>G	GRCh37
NC_000003.10:g.25753860C>G	NCBI36
NG_034108.1:g.57675G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280700.10:c.972G>C MANE Select	ENSP00000280700.5:p.Gly324=
ENST00000463611.2:c.*1063G>C	ENSP00000501918.1:n.*1063G>C
ENST00000674841.1:n.1095G>C
ENST00000675178.1:n.168-3383G>C
ENST00000675217.1:c.*345G>C	ENSP00000502195.1:n.*345G>C
ENST00000675234.1:c.*469G>C	ENSP00000502740.1:n.*469G>C
ENST00000675680.1:c.391-965G>C
ENST00000676225.1:c.882-965G>C	ENSP00000501622.1:n.882-965G>C
ENST00000280699.13:c.723G>C
ENST00000280700.9:c.972G>C	ENSP00000280700.5:p.Gly324=
ENST00000308710.9:c.963G>C	ENSP00000307980.5:p.Gly321=
ENST00000396649.7:c.972G>C	ENSP00000379886.3:p.Gly324=
ENST00000417874.6:c.846G>C	ENSP00000389888.2:p.Gly282=
ENST00000428257.5:c.972G>C	ENSP00000387430.1:p.Gly324=
ENST00000493324.5:n.996G>C
NM_001145293.1:c.972G>C	NP_001138765.1:p.Gly324=
NM_001145294.1:c.846G>C	NP_001138766.1:p.Gly282=
NM_001145295.1:c.972G>C	NP_001138767.1:p.Gly324=
NM_018297.3:c.972G>C	NP_060767.2:p.Gly324=
XM_005265316.1:c.972G>C	XP_005265373.1:p.Gly324=
XM_005265317.1:c.972G>C	XP_005265374.1:p.Gly324=
XM_011533944.1:c.741G>C	XP_011532246.1:p.Gly247=
XM_011533945.1:c.972G>C	XP_011532247.1:p.Gly324=
XR_940470.1:n.1025G>C
XR_940471.1:n.1025G>C
XM_017006839.2:c.972G>C	XP_016862328.1:p.Gly324=
XR_001740200.2:n.1025G>C
XR_002959548.1:n.1025G>C
XR_940471.2:n.1025G>C
NM_018297.4:c.972G>C MANE Select	NP_060767.2:p.Gly324=
NM_001145293.2:c.972G>C	NP_001138765.1:p.Gly324=
NM_001145294.2:c.846G>C	NP_001138766.1:p.Gly282=
NM_001145295.2:c.972G>C	NP_001138767.1:p.Gly324=