Canonical Allele Identifier: CA277164172

Gene: ALG1

Linked Data

• dbSNP Id: rs763705590
• MyVariant Identifiers: chr16:g.5131329_5131333del (hg19) ; chr16:g.5081328_5081332del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5081331_5081335del , CM000678.2:g.5081331_5081335del	GRCh38
NC_000016.9:g.5131332_5131336del , CM000678.1:g.5131332_5131336del	GRCh37
NC_000016.8:g.5071333_5071337del	NCBI36
NG_009202.1:g.14523_14527del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.3208+275_3208+279del
ENST00000682020.1:c.478+275_478+279del	ENSP00000508075.1:n.478+275_478+279del
ENST00000682206.1:c.*164+275_*164+279del	ENSP00000508285.1:n.*164+275_*164+279del
ENST00000682314.1:n.1120+275_1120+279del
ENST00000682327.1:c.544+275_544+279del	ENSP00000507058.1:n.544+275_544+279del
ENST00000682349.1:n.3214+275_3214+279del
ENST00000682703.1:n.4040+275_4040+279del
ENST00000682797.1:c.*164+275_*164+279del	ENSP00000507582.1:n.*164+275_*164+279del
ENST00000682985.1:c.583+275_583+279del	ENSP00000507598.1:n.583+275_583+279del
ENST00000683433.1:c.328+275_328+279del	ENSP00000507463.1:n.328+275_328+279del
ENST00000683685.1:n.1946+275_1946+279del
ENST00000683710.1:c.*1039+275_*1039+279del	ENSP00000506785.1:n.*1039+275_*1039+279del
ENST00000683739.1:c.739+275_739+279del	ENSP00000507002.1:n.739+275_739+279del
ENST00000683772.1:n.1116+275_1116+279del
ENST00000684008.1:c.1010+275_1010+279del	ENSP00000507962.1:n.1010+275_1010+279del
ENST00000684190.1:c.1033+275_1033+279del	ENSP00000507554.1:n.1033+275_1033+279del
ENST00000684335.1:c.962-1228_962-1224del	ENSP00000508112.1:n.962-1228_962-1224del
ENST00000262374.10:c.1072+275_1072+279del MANE Select	ENSP00000262374.5:n.1072+275_1072+279del
ENST00000650085.1:n.1896+275_1896+279del
ENST00000262374.9:c.1072+275_1072+279del	ENSP00000262374.4:n.1072+275_1072+279del
ENST00000544428.1:c.739+275_739+279del	ENSP00000440019.1:n.739+275_739+279del
ENST00000588623.5:c.739+275_739+279del	ENSP00000468118.1:n.739+275_739+279del
ENST00000591822.5:c.*973+275_*973+279del	ENSP00000467865.1:n.*973+275_*973+279del
NM_019109.4:c.1072+275_1072+279del	NP_061982.3:n.1072+275_1072+279del
XM_011522565.1:c.739+275_739+279del	XP_011520867.1:n.739+275_739+279del
NM_001330504.1:c.739+275_739+279del	NP_001317433.1:n.739+275_739+279del
XM_017023457.2:c.1033+275_1033+279del	XP_016878946.1:n.1033+275_1033+279del
XM_017023458.1:c.739+275_739+279del	XP_016878947.1:n.739+275_739+279del
XR_932882.3:n.1101+275_1101+279del
NM_019109.5:c.1072+275_1072+279del MANE Select	NP_061982.3:n.1072+275_1072+279del
NM_001330504.2:c.739+275_739+279del	NP_001317433.1:n.739+275_739+279del