Canonical Allele Identifier: CA16043011

Gene: ALG1

Linked Data

• ClinVar Variation Id: 373810
• ClinVar RCV Id: RCV000413517
• dbSNP Id: rs1057518625
• MyVariant Identifiers: chr16:g.5121919del (hg19) ; chr16:g.5071918del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5071918del , CM000678.2:g.5071918del	GRCh38
NC_000016.9:g.5121919del , CM000678.1:g.5121919del	GRCh37
NC_000016.8:g.5061920del	NCBI36
NG_009202.1:g.5110del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.76del
ENST00000682020.1:c.-55-5527del	ENSP00000508075.1:n.-55-5527del
ENST00000682206.1:c.69del	ENSP00000508285.1:p.Trp23Ter
ENST00000682314.1:n.113del
ENST00000682327.1:c.-99-3470del	ENSP00000507058.1:n.-99-3470del
ENST00000682349.1:n.76del
ENST00000682703.1:n.76del
ENST00000682797.1:c.69del	ENSP00000507582.1:p.Trp23Ter
ENST00000682985.1:c.-99-3470del	ENSP00000507598.1:n.-99-3470del
ENST00000683433.1:c.-55-5527del	ENSP00000507463.1:n.-55-5527del
ENST00000683685.1:n.113del
ENST00000683710.1:c.69del	ENSP00000506785.1:p.Trp23Ter
ENST00000683772.1:n.113del
ENST00000684008.1:c.69del	ENSP00000507962.1:p.Trp23Ter
ENST00000684190.1:c.69del	ENSP00000507554.1:p.Trp23Ter
ENST00000684335.1:c.69del	ENSP00000508112.1:p.Trp23Ter
ENST00000262374.10:c.69del MANE Select	ENSP00000262374.5:p.Trp23Ter
ENST00000650085.1:n.1013-1033del
ENST00000262374.9:c.69del	ENSP00000262374.4:p.Trp23Ter
ENST00000586840.1:c.69del	ENSP00000467538.1:p.Trp23Ter
ENST00000588623.5:c.-125-1033del	ENSP00000468118.1:n.-125-1033del
ENST00000591822.5:c.69del	ENSP00000467865.1:p.Trp23Ter
ENST00000592793.5:n.76del
NM_019109.4:c.69del	NP_061982.3:p.Trp23Ter
XR_932882.1:n.110del
XM_017023457.2:c.69del	XP_016878946.1:p.Trp23Ter
XM_017023458.1:c.-421del	XP_016878947.1:n.-421del
XR_932882.3:n.94del
NM_019109.5:c.69del MANE Select	NP_061982.3:p.Trp23Ter