Canonical Allele Identifier: CA394674503

Gene: ALG1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5083681G>A , CM000678.2:g.5083681G>A	GRCh38
NC_000016.9:g.5133682G>A , CM000678.1:g.5133682G>A	GRCh37
NC_000016.8:g.5073683G>A	NCBI36
NG_009202.1:g.16873G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019109.5:c.1188-1G>A MANE Select	NP_061982.3:n.1188-1G>A
ENST00000262374.10:c.1188-1G>A MANE Select	ENSP00000262374.5:n.1188-1G>A
NM_001330504.1:c.855-1G>A	NP_001317433.1:n.855-1G>A
NM_001330504.2:c.855-1G>A	NP_001317433.1:n.855-1G>A
NM_019109.4:c.1188-1G>A	NP_061982.3:n.1188-1G>A
ENST00000262374.9:c.1188-1G>A	ENSP00000262374.4:n.1188-1G>A
ENST00000544428.1:c.855-1G>A	ENSP00000440019.1:n.855-1G>A
ENST00000588623.5:c.855-1G>A	ENSP00000468118.1:n.855-1G>A
ENST00000591822.5:c.*1089-1G>A	ENSP00000467865.1:n.*1089-1G>A
ENST00000592793.6:n.3324-1G>A
ENST00000650085.1:n.2012-1G>A
ENST00000682020.1:c.594-1G>A	ENSP00000508075.1:n.594-1G>A
ENST00000682206.1:c.*283-1G>A	ENSP00000508285.1:n.*283-1G>A
ENST00000682314.1:n.2243G>A
ENST00000682327.1:c.660-1G>A	ENSP00000507058.1:n.660-1G>A
ENST00000682349.1:n.3330-1G>A
ENST00000682703.1:n.5163G>A
ENST00000682797.1:c.*280-1G>A	ENSP00000507582.1:n.*280-1G>A
ENST00000682985.1:c.699-1G>A	ENSP00000507598.1:n.699-1G>A
ENST00000683433.1:c.447-1G>A	ENSP00000507463.1:n.447-1G>A
ENST00000683685.1:n.3069G>A
ENST00000683710.1:c.*1155-1G>A	ENSP00000506785.1:n.*1155-1G>A
ENST00000683739.1:c.855-1G>A	ENSP00000507002.1:n.855-1G>A
ENST00000683772.1:n.2239G>A
ENST00000684008.1:c.1126-1G>A	ENSP00000507962.1:n.1126-1G>A
ENST00000684190.1:c.1149-1G>A	ENSP00000507554.1:n.1149-1G>A
ENST00000684335.1:c.1077-1G>A	ENSP00000508112.1:n.1077-1G>A
XM_011522565.1:c.855-1G>A	XP_011520867.1:n.855-1G>A
XM_017023457.2:c.1149-1G>A	XP_016878946.1:n.1149-1G>A
XM_017023458.1:c.855-1G>A	XP_016878947.1:n.855-1G>A
XR_932882.3:n.1217-1G>A