Canonical Allele Identifier: CA2631591516

Gene: ALG1

Linked Data

• gnomAD v4: 16-5081147-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5081151_5081152del , CM000678.2:g.5081151_5081152del	GRCh38
NC_000016.9:g.5131152_5131153del , CM000678.1:g.5131152_5131153del	GRCh37
NC_000016.8:g.5071153_5071154del	NCBI36
NG_009202.1:g.14343_14344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.3208+95_3208+96del
ENST00000682020.1:c.478+95_478+96del	ENSP00000508075.1:n.478+95_478+96del
ENST00000682206.1:c.*164+95_*164+96del	ENSP00000508285.1:n.*164+95_*164+96del
ENST00000682314.1:n.1120+95_1120+96del
ENST00000682327.1:c.544+95_544+96del	ENSP00000507058.1:n.544+95_544+96del
ENST00000682349.1:n.3214+95_3214+96del
ENST00000682703.1:n.4040+95_4040+96del
ENST00000682797.1:c.*164+95_*164+96del	ENSP00000507582.1:n.*164+95_*164+96del
ENST00000682985.1:c.583+95_583+96del	ENSP00000507598.1:n.583+95_583+96del
ENST00000683433.1:c.328+95_328+96del	ENSP00000507463.1:n.328+95_328+96del
ENST00000683685.1:n.1946+95_1946+96del
ENST00000683710.1:c.*1039+95_*1039+96del	ENSP00000506785.1:n.*1039+95_*1039+96del
ENST00000683739.1:c.739+95_739+96del	ENSP00000507002.1:n.739+95_739+96del
ENST00000683772.1:n.1116+95_1116+96del
ENST00000684008.1:c.1010+95_1010+96del	ENSP00000507962.1:n.1010+95_1010+96del
ENST00000684190.1:c.1033+95_1033+96del	ENSP00000507554.1:n.1033+95_1033+96del
ENST00000684335.1:c.961+1344_961+1345del	ENSP00000508112.1:n.961+1344_961+1345del
ENST00000262374.10:c.1072+95_1072+96del MANE Select	ENSP00000262374.5:n.1072+95_1072+96del
ENST00000650085.1:n.1896+95_1896+96del
ENST00000262374.9:c.1072+95_1072+96del	ENSP00000262374.4:n.1072+95_1072+96del
ENST00000544428.1:c.739+95_739+96del	ENSP00000440019.1:n.739+95_739+96del
ENST00000588623.5:c.739+95_739+96del	ENSP00000468118.1:n.739+95_739+96del
ENST00000591822.5:c.*973+95_*973+96del	ENSP00000467865.1:n.*973+95_*973+96del
NM_019109.4:c.1072+95_1072+96del	NP_061982.3:n.1072+95_1072+96del
XM_011522565.1:c.739+95_739+96del	XP_011520867.1:n.739+95_739+96del
NM_001330504.1:c.739+95_739+96del	NP_001317433.1:n.739+95_739+96del
XM_017023457.2:c.1033+95_1033+96del	XP_016878946.1:n.1033+95_1033+96del
XM_017023458.1:c.739+95_739+96del	XP_016878947.1:n.739+95_739+96del
XR_932882.3:n.1101+95_1101+96del
NM_019109.5:c.1072+95_1072+96del MANE Select	NP_061982.3:n.1072+95_1072+96del
NM_001330504.2:c.739+95_739+96del	NP_001317433.1:n.739+95_739+96del