Canonical Allele Identifier: CA7889670

Gene: ALG1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5071944C>A , CM000678.2:g.5071944C>A	GRCh38
NC_000016.9:g.5121945C>A , CM000678.1:g.5121945C>A	GRCh37
NC_000016.8:g.5061946C>A	NCBI36
NG_009202.1:g.5136C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019109.5:c.95C>A MANE Select	NP_061982.3:p.Ala32Asp
ENST00000262374.10:c.95C>A MANE Select	ENSP00000262374.5:p.Ala32Asp
NM_019109.4:c.95C>A	NP_061982.3:p.Ala32Asp
ENST00000262374.9:c.95C>A	ENSP00000262374.4:p.Ala32Asp
ENST00000586840.1:c.95C>A	ENSP00000467538.1:p.Ala32Asp
ENST00000588623.5:c.-125-1007C>A	ENSP00000468118.1:n.-125-1007C>A
ENST00000591822.5:c.95C>A	ENSP00000467865.1:p.Ala32Asp
ENST00000592793.5:n.102C>A
ENST00000592793.6:n.102C>A
ENST00000650085.1:n.1013-1007C>A
ENST00000682020.1:c.-55-5501C>A	ENSP00000508075.1:n.-55-5501C>A
ENST00000682206.1:c.95C>A	ENSP00000508285.1:p.Ala32Asp
ENST00000682314.1:n.139C>A
ENST00000682327.1:c.-99-3444C>A	ENSP00000507058.1:n.-99-3444C>A
ENST00000682349.1:n.102C>A
ENST00000682703.1:n.102C>A
ENST00000682797.1:c.95C>A	ENSP00000507582.1:p.Ala32Asp
ENST00000682985.1:c.-99-3444C>A	ENSP00000507598.1:n.-99-3444C>A
ENST00000683433.1:c.-55-5501C>A	ENSP00000507463.1:n.-55-5501C>A
ENST00000683685.1:n.139C>A
ENST00000683710.1:c.95C>A	ENSP00000506785.1:p.Ala32Asp
ENST00000683772.1:n.139C>A
ENST00000684008.1:c.95C>A	ENSP00000507962.1:p.Ala32Asp
ENST00000684190.1:c.95C>A	ENSP00000507554.1:p.Ala32Asp
ENST00000684335.1:c.95C>A	ENSP00000508112.1:p.Ala32Asp
XM_017023457.2:c.95C>A	XP_016878946.1:p.Ala32Asp
XM_017023458.1:c.-395C>A	XP_016878947.1:n.-395C>A
XR_932882.1:n.136C>A
XR_932882.3:n.120C>A