Canonical Allele Identifier: CA2203686085

Gene: ALG1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5081170_5081171delinsGC , CM000678.2:g.5081170_5081171delinsGC	GRCh38
NC_000016.9:g.5131171_5131172delinsGC , CM000678.1:g.5131171_5131172delinsGC	GRCh37
NC_000016.8:g.5071172_5071173delinsGC	NCBI36
NG_009202.1:g.14362_14363delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.3208+114_3208+115delinsGC
ENST00000682020.1:c.478+114_478+115delinsGC	ENSP00000508075.1:n.478+114_478+115delinsGC
ENST00000682206.1:c.*164+114_*164+115delinsGC	ENSP00000508285.1:n.*164+114_*164+115delinsGC
ENST00000682314.1:n.1120+114_1120+115delinsGC
ENST00000682327.1:c.544+114_544+115delinsGC	ENSP00000507058.1:n.544+114_544+115delinsGC
ENST00000682349.1:n.3214+114_3214+115delinsGC
ENST00000682703.1:n.4040+114_4040+115delinsGC
ENST00000682797.1:c.*164+114_*164+115delinsGC	ENSP00000507582.1:n.*164+114_*164+115delinsGC
ENST00000682985.1:c.583+114_583+115delinsGC	ENSP00000507598.1:n.583+114_583+115delinsGC
ENST00000683433.1:c.328+114_328+115delinsGC	ENSP00000507463.1:n.328+114_328+115delinsGC
ENST00000683685.1:n.1946+114_1946+115delinsGC
ENST00000683710.1:c.*1039+114_*1039+115delinsGC	ENSP00000506785.1:n.*1039+114_*1039+115delinsGC
ENST00000683739.1:c.739+114_739+115delinsGC	ENSP00000507002.1:n.739+114_739+115delinsGC
ENST00000683772.1:n.1116+114_1116+115delinsGC
ENST00000684008.1:c.1010+114_1010+115delinsGC	ENSP00000507962.1:n.1010+114_1010+115delinsGC
ENST00000684190.1:c.1033+114_1033+115delinsGC	ENSP00000507554.1:n.1033+114_1033+115delinsGC
ENST00000684335.1:c.961+1363_961+1364delinsGC	ENSP00000508112.1:n.961+1363_961+1364delinsGC
ENST00000262374.10:c.1072+114_1072+115delinsGC MANE Select	ENSP00000262374.5:n.1072+114_1072+115delinsGC
ENST00000650085.1:n.1896+114_1896+115delinsGC
ENST00000262374.9:c.1072+114_1072+115delinsGC	ENSP00000262374.4:n.1072+114_1072+115delinsGC
ENST00000544428.1:c.739+114_739+115delinsGC	ENSP00000440019.1:n.739+114_739+115delinsGC
ENST00000588623.5:c.739+114_739+115delinsGC	ENSP00000468118.1:n.739+114_739+115delinsGC
ENST00000591822.5:c.*973+114_*973+115delinsGC	ENSP00000467865.1:n.*973+114_*973+115delinsGC
NM_019109.4:c.1072+114_1072+115delinsGC	NP_061982.3:n.1072+114_1072+115delinsGC
XM_011522565.1:c.739+114_739+115delinsGC	XP_011520867.1:n.739+114_739+115delinsGC
NM_001330504.1:c.739+114_739+115delinsGC	NP_001317433.1:n.739+114_739+115delinsGC
XM_017023457.2:c.1033+114_1033+115delinsGC	XP_016878946.1:n.1033+114_1033+115delinsGC
XM_017023458.1:c.739+114_739+115delinsGC	XP_016878947.1:n.739+114_739+115delinsGC
XR_932882.3:n.1101+114_1101+115delinsGC
NM_019109.5:c.1072+114_1072+115delinsGC MANE Select	NP_061982.3:n.1072+114_1072+115delinsGC
NM_001330504.2:c.739+114_739+115delinsGC	NP_001317433.1:n.739+114_739+115delinsGC