Canonical Allele Identifier: CA394681688

Gene: ALG1

Linked Data

• MyVariant Identifiers: chr16:g.5128765C>A (hg19) ; chr16:g.5078764C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5078764C>A , CM000678.2:g.5078764C>A	GRCh38
NC_000016.9:g.5128765C>A , CM000678.1:g.5128765C>A	GRCh37
NC_000016.8:g.5068766C>A	NCBI36
NG_009202.1:g.11956C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.2886C>A
ENST00000682020.1:c.154C>A	ENSP00000508075.1:p.Pro52Thr
ENST00000682206.1:c.748C>A	ENSP00000508285.1:p.Pro250Thr
ENST00000682314.1:n.792C>A
ENST00000682327.1:c.259C>A	ENSP00000507058.1:p.Pro87Thr
ENST00000682349.1:n.2886C>A
ENST00000682703.1:n.2886C>A
ENST00000682797.1:c.748C>A	ENSP00000507582.1:p.Pro250Thr
ENST00000682985.1:c.259C>A	ENSP00000507598.1:p.Pro87Thr
ENST00000683433.1:c.43C>A	ENSP00000507463.1:p.Pro15Thr
ENST00000683685.1:n.792C>A
ENST00000683710.1:c.*711C>A	ENSP00000506785.1:n.*711C>A
ENST00000683739.1:c.415C>A	ENSP00000507002.1:p.Pro139Thr
ENST00000683772.1:n.792C>A
ENST00000684008.1:c.682C>A	ENSP00000507962.1:p.Pro228Thr
ENST00000684190.1:c.748C>A	ENSP00000507554.1:p.Pro250Thr
ENST00000684335.1:c.748C>A	ENSP00000508112.1:p.Pro250Thr
ENST00000262374.10:c.748C>A MANE Select	ENSP00000262374.5:p.Pro250Thr
ENST00000650085.1:n.1568C>A
ENST00000262374.9:c.748C>A	ENSP00000262374.4:p.Pro250Thr
ENST00000544428.1:c.415C>A	ENSP00000440019.1:p.Pro139Thr
ENST00000588623.5:c.415C>A	ENSP00000468118.1:p.Pro139Thr
ENST00000591783.5:c.415C>A	ENSP00000464700.1:p.Pro139Thr
ENST00000591822.5:c.*649C>A	ENSP00000467865.1:n.*649C>A
NM_019109.4:c.748C>A	NP_061982.3:p.Pro250Thr
XM_011522565.1:c.415C>A	XP_011520867.1:p.Pro139Thr
XR_932882.1:n.789C>A
NM_001330504.1:c.415C>A	NP_001317433.1:p.Pro139Thr
XM_017023457.2:c.748C>A	XP_016878946.1:p.Pro250Thr
XM_017023458.1:c.415C>A	XP_016878947.1:p.Pro139Thr
XR_932882.3:n.773C>A
NM_019109.5:c.748C>A MANE Select	NP_061982.3:p.Pro250Thr
NM_001330504.2:c.415C>A	NP_001317433.1:p.Pro139Thr