Canonical Allele Identifier: CA7889951

Gene: ALG1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5077929C>T , CM000678.2:g.5077929C>T	GRCh38
NC_000016.9:g.5127930C>T , CM000678.1:g.5127930C>T	GRCh37
NC_000016.8:g.5067931C>T	NCBI36
NG_009202.1:g.11121C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_019109.5:c.652C>T MANE Select	NP_061982.3:p.Pro218Ser
ENST00000262374.10:c.652C>T MANE Select	ENSP00000262374.5:p.Pro218Ser
NM_001330504.1:c.319C>T	NP_001317433.1:p.Pro107Ser
NM_001330504.2:c.319C>T	NP_001317433.1:p.Pro107Ser
NM_019109.4:c.652C>T	NP_061982.3:p.Pro218Ser
ENST00000262374.9:c.652C>T	ENSP00000262374.4:p.Pro218Ser
ENST00000544428.1:c.319C>T	ENSP00000440019.1:p.Pro107Ser
ENST00000588623.5:c.319C>T	ENSP00000468118.1:p.Pro107Ser
ENST00000591783.5:c.319C>T	ENSP00000464700.1:p.Pro107Ser
ENST00000591822.5:c.*553C>T	ENSP00000467865.1:n.*553C>T
ENST00000592793.6:n.2790C>T
ENST00000650085.1:n.1472C>T
ENST00000682020.1:c.58C>T	ENSP00000508075.1:p.Pro20Ser
ENST00000682206.1:c.652C>T	ENSP00000508285.1:p.Pro218Ser
ENST00000682314.1:n.696C>T
ENST00000682327.1:c.163C>T	ENSP00000507058.1:p.Pro55Ser
ENST00000682349.1:n.2790C>T
ENST00000682703.1:n.2790C>T
ENST00000682797.1:c.652C>T	ENSP00000507582.1:p.Pro218Ser
ENST00000682985.1:c.163C>T	ENSP00000507598.1:p.Pro55Ser
ENST00000683433.1:c.35+395C>T	ENSP00000507463.1:n.35+395C>T
ENST00000683685.1:n.696C>T
ENST00000683710.1:c.*615C>T	ENSP00000506785.1:n.*615C>T
ENST00000683739.1:c.319C>T	ENSP00000507002.1:p.Pro107Ser
ENST00000683772.1:n.696C>T
ENST00000684008.1:c.586C>T	ENSP00000507962.1:p.Pro196Ser
ENST00000684190.1:c.652C>T	ENSP00000507554.1:p.Pro218Ser
ENST00000684335.1:c.652C>T	ENSP00000508112.1:p.Pro218Ser
XM_011522565.1:c.319C>T	XP_011520867.1:p.Pro107Ser
XM_017023457.2:c.652C>T	XP_016878946.1:p.Pro218Ser
XM_017023458.1:c.319C>T	XP_016878947.1:p.Pro107Ser
XR_932882.1:n.693C>T
XR_932882.3:n.677C>T