Canonical Allele Identifier: CA2203685541

Gene: ALG1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5080866_5080867delinsAG , CM000678.2:g.5080866_5080867delinsAG	GRCh38
NC_000016.9:g.5130867_5130868delinsAG , CM000678.1:g.5130867_5130868delinsAG	GRCh37
NC_000016.8:g.5070868_5070869delinsAG	NCBI36
NG_009202.1:g.14058_14059delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.3098-80_3098-79delinsAG
ENST00000682020.1:c.368-80_368-79delinsAG	ENSP00000508075.1:n.368-80_368-79delinsAG
ENST00000682206.1:c.*54-80_*54-79delinsAG	ENSP00000508285.1:n.*54-80_*54-79delinsAG
ENST00000682314.1:n.1010-80_1010-79delinsAG
ENST00000682327.1:c.434-80_434-79delinsAG	ENSP00000507058.1:n.434-80_434-79delinsAG
ENST00000682349.1:n.3104-80_3104-79delinsAG
ENST00000682703.1:n.3930-80_3930-79delinsAG
ENST00000682797.1:c.*54-80_*54-79delinsAG	ENSP00000507582.1:n.*54-80_*54-79delinsAG
ENST00000682985.1:c.473-80_473-79delinsAG	ENSP00000507598.1:n.473-80_473-79delinsAG
ENST00000683433.1:c.218-80_218-79delinsAG	ENSP00000507463.1:n.218-80_218-79delinsAG
ENST00000683685.1:n.1836-80_1836-79delinsAG
ENST00000683710.1:c.*929-80_*929-79delinsAG	ENSP00000506785.1:n.*929-80_*929-79delinsAG
ENST00000683739.1:c.629-80_629-79delinsAG	ENSP00000507002.1:n.629-80_629-79delinsAG
ENST00000683772.1:n.1006-80_1006-79delinsAG
ENST00000684008.1:c.900-80_900-79delinsAG	ENSP00000507962.1:n.900-80_900-79delinsAG
ENST00000684190.1:c.923-80_923-79delinsAG	ENSP00000507554.1:n.923-80_923-79delinsAG
ENST00000684335.1:c.961+1059_961+1060delinsAG	ENSP00000508112.1:n.961+1059_961+1060delinsAG
ENST00000262374.10:c.962-80_962-79delinsAG MANE Select	ENSP00000262374.5:n.962-80_962-79delinsAG
ENST00000650085.1:n.1786-80_1786-79delinsAG
ENST00000262374.9:c.962-80_962-79delinsAG	ENSP00000262374.4:n.962-80_962-79delinsAG
ENST00000544428.1:c.629-80_629-79delinsAG	ENSP00000440019.1:n.629-80_629-79delinsAG
ENST00000588623.5:c.629-80_629-79delinsAG	ENSP00000468118.1:n.629-80_629-79delinsAG
ENST00000591822.5:c.*863-80_*863-79delinsAG	ENSP00000467865.1:n.*863-80_*863-79delinsAG
NM_019109.4:c.962-80_962-79delinsAG	NP_061982.3:n.962-80_962-79delinsAG
XM_011522565.1:c.629-80_629-79delinsAG	XP_011520867.1:n.629-80_629-79delinsAG
XR_932882.1:n.1007-80_1007-79delinsAG
NM_001330504.1:c.629-80_629-79delinsAG	NP_001317433.1:n.629-80_629-79delinsAG
XM_017023457.2:c.923-80_923-79delinsAG	XP_016878946.1:n.923-80_923-79delinsAG
XM_017023458.1:c.629-80_629-79delinsAG	XP_016878947.1:n.629-80_629-79delinsAG
XR_932882.3:n.991-80_991-79delinsAG
NM_019109.5:c.962-80_962-79delinsAG MANE Select	NP_061982.3:n.962-80_962-79delinsAG
NM_001330504.2:c.629-80_629-79delinsAG	NP_001317433.1:n.629-80_629-79delinsAG