Canonical Allele Identifier: CA493335482

Gene: ALG1

Linked Data

• dbSNP Id: rs1957033876
• MyVariant Identifiers: chr16:g.5132561G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5082560G>A , CM000678.2:g.5082560G>A	GRCh38
NC_000016.9:g.5132561G>A , CM000678.1:g.5132561G>A	GRCh37
NC_000016.8:g.5072562G>A	NCBI36
NG_009202.1:g.15752G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.3210G>A
ENST00000682020.1:c.480G>A	ENSP00000508075.1:p.Gly160=
ENST00000682206.1:c.*169G>A	ENSP00000508285.1:n.*169G>A
ENST00000682314.1:n.1122G>A
ENST00000682327.1:c.546G>A	ENSP00000507058.1:p.Gly182=
ENST00000682349.1:n.3216G>A
ENST00000682703.1:n.4042G>A
ENST00000682797.1:c.*166G>A	ENSP00000507582.1:n.*166G>A
ENST00000682985.1:c.585G>A	ENSP00000507598.1:p.Gly195=
ENST00000683433.1:c.333G>A	ENSP00000507463.1:p.Gly111=
ENST00000683685.1:n.1948G>A
ENST00000683710.1:c.*1041G>A	ENSP00000506785.1:n.*1041G>A
ENST00000683739.1:c.741G>A	ENSP00000507002.1:p.Gly247=
ENST00000683772.1:n.1118G>A
ENST00000684008.1:c.1012G>A	ENSP00000507962.1:n.1012G>A
ENST00000684190.1:c.1035G>A	ENSP00000507554.1:p.Gly345=
ENST00000684335.1:c.963G>A	ENSP00000508112.1:p.Gly321=
ENST00000262374.10:c.1074G>A MANE Select	ENSP00000262374.5:p.Gly358=
ENST00000650085.1:n.1898G>A
ENST00000262374.9:c.1074G>A	ENSP00000262374.4:p.Gly358=
ENST00000544428.1:c.741G>A	ENSP00000440019.1:p.Gly247=
ENST00000588623.5:c.741G>A	ENSP00000468118.1:p.Gly247=
ENST00000591822.5:c.*975G>A	ENSP00000467865.1:n.*975G>A
NM_019109.4:c.1074G>A	NP_061982.3:p.Gly358=
XM_011522565.1:c.741G>A	XP_011520867.1:p.Gly247=
NM_001330504.1:c.741G>A	NP_001317433.1:p.Gly247=
XM_017023457.2:c.1035G>A	XP_016878946.1:p.Gly345=
XM_017023458.1:c.741G>A	XP_016878947.1:p.Gly247=
XR_932882.3:n.1103G>A
NM_019109.5:c.1074G>A MANE Select	NP_061982.3:p.Gly358=
NM_001330504.2:c.741G>A	NP_001317433.1:p.Gly247=