Canonical Allele Identifier: CA2631591449

Gene: ALG1

Linked Data

• gnomAD v4: 16-5081110-G-GGTAACTGGGGGGGGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5081110_5081111insGTAACTGGGGGGGGGGC , CM000678.2:g.5081110_5081111insGTAACTGGGGGGGGGGC	GRCh38
NC_000016.9:g.5131111_5131112insGTAACTGGGGGGGGGGC , CM000678.1:g.5131111_5131112insGTAACTGGGGGGGGGGC	GRCh37
NC_000016.8:g.5071112_5071113insGTAACTGGGGGGGGGGC	NCBI36
NG_009202.1:g.14302_14303insGTAACTGGGGGGGGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.3208+54_3208+55insGTAACTGGGGGGGGGGC
ENST00000682020.1:c.478+54_478+55insGTAACTGGGGGGGGGGC	ENSP00000508075.1:n.478+54_478+55insGTAACTGGGGGGGGGGC
ENST00000682206.1:c.*164+54_*164+55insGTAACTGGGGGGGGGGC	ENSP00000508285.1:n.*164+54_*164+55insGTAACTGGGGGGGGGGC
ENST00000682314.1:n.1120+54_1120+55insGTAACTGGGGGGGGGGC
ENST00000682327.1:c.544+54_544+55insGTAACTGGGGGGGGGGC	ENSP00000507058.1:n.544+54_544+55insGTAACTGGGGGGGGGGC
ENST00000682349.1:n.3214+54_3214+55insGTAACTGGGGGGGGGGC
ENST00000682703.1:n.4040+54_4040+55insGTAACTGGGGGGGGGGC
ENST00000682797.1:c.*164+54_*164+55insGTAACTGGGGGGGGGGC	ENSP00000507582.1:n.*164+54_*164+55insGTAACTGGGGGGGGGGC
ENST00000682985.1:c.583+54_583+55insGTAACTGGGGGGGGGGC	ENSP00000507598.1:n.583+54_583+55insGTAACTGGGGGGGGGGC
ENST00000683433.1:c.328+54_328+55insGTAACTGGGGGGGGGGC	ENSP00000507463.1:n.328+54_328+55insGTAACTGGGGGGGGGGC
ENST00000683685.1:n.1946+54_1946+55insGTAACTGGGGGGGGGGC
ENST00000683710.1:c.*1039+54_*1039+55insGTAACTGGGGGGGGGGC	ENSP00000506785.1:n.*1039+54_*1039+55insGTAACTGGGGGGGGGGC
ENST00000683739.1:c.739+54_739+55insGTAACTGGGGGGGGGGC	ENSP00000507002.1:n.739+54_739+55insGTAACTGGGGGGGGGGC
ENST00000683772.1:n.1116+54_1116+55insGTAACTGGGGGGGGGGC
ENST00000684008.1:c.1010+54_1010+55insGTAACTGGGGGGGGGGC	ENSP00000507962.1:n.1010+54_1010+55insGTAACTGGGGGGGGGGC
ENST00000684190.1:c.1033+54_1033+55insGTAACTGGGGGGGGGGC	ENSP00000507554.1:n.1033+54_1033+55insGTAACTGGGGGGGGGGC
ENST00000684335.1:c.961+1303_961+1304insGTAACTGGGGGGGGGGC	ENSP00000508112.1:n.961+1303_961+1304insGTAACTGGGGGGGGGGC
ENST00000262374.10:c.1072+54_1072+55insGTAACTGGGGGGGGGGC MANE Select	ENSP00000262374.5:n.1072+54_1072+55insGTAACTGGGGGGGGGGC
ENST00000650085.1:n.1896+54_1896+55insGTAACTGGGGGGGGGGC
ENST00000262374.9:c.1072+54_1072+55insGTAACTGGGGGGGGGGC	ENSP00000262374.4:n.1072+54_1072+55insGTAACTGGGGGGGGGGC
ENST00000544428.1:c.739+54_739+55insGTAACTGGGGGGGGGGC	ENSP00000440019.1:n.739+54_739+55insGTAACTGGGGGGGGGGC
ENST00000588623.5:c.739+54_739+55insGTAACTGGGGGGGGGGC	ENSP00000468118.1:n.739+54_739+55insGTAACTGGGGGGGGGGC
ENST00000591822.5:c.*973+54_*973+55insGTAACTGGGGGGGGGGC	ENSP00000467865.1:n.*973+54_*973+55insGTAACTGGGGGGGGGGC
NM_019109.4:c.1072+54_1072+55insGTAACTGGGGGGGGGGC	NP_061982.3:n.1072+54_1072+55insGTAACTGGGGGGGGGGC
XM_011522565.1:c.739+54_739+55insGTAACTGGGGGGGGGGC	XP_011520867.1:n.739+54_739+55insGTAACTGGGGGGGGGGC
NM_001330504.1:c.739+54_739+55insGTAACTGGGGGGGGGGC	NP_001317433.1:n.739+54_739+55insGTAACTGGGGGGGGGGC
XM_017023457.2:c.1033+54_1033+55insGTAACTGGGGGGGGGGC	XP_016878946.1:n.1033+54_1033+55insGTAACTGGGGGGGGGGC
XM_017023458.1:c.739+54_739+55insGTAACTGGGGGGGGGGC	XP_016878947.1:n.739+54_739+55insGTAACTGGGGGGGGGGC
XR_932882.3:n.1101+54_1101+55insGTAACTGGGGGGGGGGC
NM_019109.5:c.1072+54_1072+55insGTAACTGGGGGGGGGGC MANE Select	NP_061982.3:n.1072+54_1072+55insGTAACTGGGGGGGGGGC
NM_001330504.2:c.739+54_739+55insGTAACTGGGGGGGGGGC	NP_001317433.1:n.739+54_739+55insGTAACTGGGGGGGGGGC