Canonical Allele Identifier: CA394681701

Gene: ALG1

Linked Data

• MyVariant Identifiers: chr16:g.5128771G>C (hg19) ; chr16:g.5078770G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5078770G>C , CM000678.2:g.5078770G>C	GRCh38
NC_000016.9:g.5128771G>C , CM000678.1:g.5128771G>C	GRCh37
NC_000016.8:g.5068772G>C	NCBI36
NG_009202.1:g.11962G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.2892G>C
ENST00000682020.1:c.160G>C	ENSP00000508075.1:p.Asp54His
ENST00000682206.1:c.754G>C	ENSP00000508285.1:p.Asp252His
ENST00000682314.1:n.798G>C
ENST00000682327.1:c.265G>C	ENSP00000507058.1:p.Asp89His
ENST00000682349.1:n.2892G>C
ENST00000682703.1:n.2892G>C
ENST00000682797.1:c.754G>C	ENSP00000507582.1:p.Asp252His
ENST00000682985.1:c.265G>C	ENSP00000507598.1:p.Asp89His
ENST00000683433.1:c.49G>C	ENSP00000507463.1:p.Asp17His
ENST00000683685.1:n.798G>C
ENST00000683710.1:c.*717G>C	ENSP00000506785.1:n.*717G>C
ENST00000683739.1:c.421G>C	ENSP00000507002.1:p.Asp141His
ENST00000683772.1:n.798G>C
ENST00000684008.1:c.688G>C	ENSP00000507962.1:p.Asp230His
ENST00000684190.1:c.754G>C	ENSP00000507554.1:p.Asp252His
ENST00000684335.1:c.754G>C	ENSP00000508112.1:p.Asp252His
ENST00000262374.10:c.754G>C MANE Select	ENSP00000262374.5:p.Asp252His
ENST00000650085.1:n.1574G>C
ENST00000262374.9:c.754G>C	ENSP00000262374.4:p.Asp252His
ENST00000544428.1:c.421G>C	ENSP00000440019.1:p.Asp141His
ENST00000588623.5:c.421G>C	ENSP00000468118.1:p.Asp141His
ENST00000591783.5:c.421G>C	ENSP00000464700.1:p.Asp141His
ENST00000591822.5:c.*655G>C	ENSP00000467865.1:n.*655G>C
NM_019109.4:c.754G>C	NP_061982.3:p.Asp252His
XM_011522565.1:c.421G>C	XP_011520867.1:p.Asp141His
XR_932882.1:n.795G>C
NM_001330504.1:c.421G>C	NP_001317433.1:p.Asp141His
XM_017023457.2:c.754G>C	XP_016878946.1:p.Asp252His
XM_017023458.1:c.421G>C	XP_016878947.1:p.Asp141His
XR_932882.3:n.779G>C
NM_019109.5:c.754G>C MANE Select	NP_061982.3:p.Asp252His
NM_001330504.2:c.421G>C	NP_001317433.1:p.Asp141His