Canonical Allele Identifier: CA493335323

Gene: ALG1

Linked Data

• ClinVar Variation Id: 2696396
• ClinVar RCV Id: RCV003502852
• MyVariant Identifiers: chr16:g.5128851C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5078850C>T , CM000678.2:g.5078850C>T	GRCh38
NC_000016.9:g.5128851C>T , CM000678.1:g.5128851C>T	GRCh37
NC_000016.8:g.5068852C>T	NCBI36
NG_009202.1:g.12042C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000592793.6:n.2972C>T
ENST00000682020.1:c.240C>T	ENSP00000508075.1:p.Ala80=
ENST00000682206.1:c.834C>T	ENSP00000508285.1:p.Ala278=
ENST00000682314.1:n.878C>T
ENST00000682327.1:c.345C>T	ENSP00000507058.1:p.Ala115=
ENST00000682349.1:n.2972C>T
ENST00000682703.1:n.2972C>T
ENST00000682797.1:c.834C>T	ENSP00000507582.1:p.Ala278=
ENST00000682985.1:c.345C>T	ENSP00000507598.1:p.Ala115=
ENST00000683433.1:c.129C>T	ENSP00000507463.1:p.Ala43=
ENST00000683685.1:n.878C>T
ENST00000683710.1:c.*797C>T	ENSP00000506785.1:n.*797C>T
ENST00000683739.1:c.501C>T	ENSP00000507002.1:p.Ala167=
ENST00000683772.1:n.878C>T
ENST00000684008.1:c.768C>T	ENSP00000507962.1:p.Ala256=
ENST00000684190.1:c.834C>T	ENSP00000507554.1:p.Ala278=
ENST00000684335.1:c.834C>T	ENSP00000508112.1:p.Ala278=
ENST00000262374.10:c.834C>T MANE Select	ENSP00000262374.5:p.Ala278=
ENST00000650085.1:n.1654C>T
ENST00000262374.9:c.834C>T	ENSP00000262374.4:p.Ala278=
ENST00000544428.1:c.501C>T	ENSP00000440019.1:p.Ala167=
ENST00000588623.5:c.501C>T	ENSP00000468118.1:p.Ala167=
ENST00000591783.5:c.501C>T	ENSP00000464700.1:p.Ala167=
ENST00000591822.5:c.*735C>T	ENSP00000467865.1:n.*735C>T
NM_019109.4:c.834C>T	NP_061982.3:p.Ala278=
XM_011522565.1:c.501C>T	XP_011520867.1:p.Ala167=
XR_932882.1:n.875C>T
NM_001330504.1:c.501C>T	NP_001317433.1:p.Ala167=
XM_017023457.2:c.834C>T	XP_016878946.1:p.Ala278=
XM_017023458.1:c.501C>T	XP_016878947.1:p.Ala167=
XR_932882.3:n.859C>T
NM_019109.5:c.834C>T MANE Select	NP_061982.3:p.Ala278=
NM_001330504.2:c.501C>T	NP_001317433.1:p.Ala167=