Canonical Allele Identifier: CA2203686047

Gene: ALG1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5081154C= , CM000678.2:g.5081154C=	GRCh38
NC_000016.9:g.5131155C= , CM000678.1:g.5131155C=	GRCh37
NC_000016.8:g.5071156C=	NCBI36
NG_009202.1:g.14346C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592793.6:n.3208+98C=
ENST00000682020.1:c.478+98C=	ENSP00000508075.1:n.478+98C=
ENST00000682206.1:c.*164+98C=	ENSP00000508285.1:n.*164+98C=
ENST00000682314.1:n.1120+98C=
ENST00000682327.1:c.544+98C=	ENSP00000507058.1:n.544+98C=
ENST00000682349.1:n.3214+98C=
ENST00000682703.1:n.4040+98C=
ENST00000682797.1:c.*164+98C=	ENSP00000507582.1:n.*164+98C=
ENST00000682985.1:c.583+98C=	ENSP00000507598.1:n.583+98C=
ENST00000683433.1:c.328+98C=	ENSP00000507463.1:n.328+98C=
ENST00000683685.1:n.1946+98C=
ENST00000683710.1:c.*1039+98C=	ENSP00000506785.1:n.*1039+98C=
ENST00000683739.1:c.739+98C=	ENSP00000507002.1:n.739+98C=
ENST00000683772.1:n.1116+98C=
ENST00000684008.1:c.1010+98C=	ENSP00000507962.1:n.1010+98C=
ENST00000684190.1:c.1033+98C=	ENSP00000507554.1:n.1033+98C=
ENST00000684335.1:c.961+1347C=	ENSP00000508112.1:n.961+1347C=
ENST00000262374.10:c.1072+98C= MANE Select	ENSP00000262374.5:n.1072+98C=
ENST00000650085.1:n.1896+98C=
ENST00000262374.9:c.1072+98C=	ENSP00000262374.4:n.1072+98C=
ENST00000544428.1:c.739+98C=	ENSP00000440019.1:n.739+98C=
ENST00000588623.5:c.739+98C=	ENSP00000468118.1:n.739+98C=
ENST00000591822.5:c.*973+98C=	ENSP00000467865.1:n.*973+98C=
NM_019109.4:c.1072+98C=	NP_061982.3:n.1072+98C=
XM_011522565.1:c.739+98C=	XP_011520867.1:n.739+98C=
NM_001330504.1:c.739+98C=	NP_001317433.1:n.739+98C=
XM_017023457.2:c.1033+98C=	XP_016878946.1:n.1033+98C=
XM_017023458.1:c.739+98C=	XP_016878947.1:n.739+98C=
XR_932882.3:n.1101+98C=
NM_019109.5:c.1072+98C= MANE Select	NP_061982.3:n.1072+98C=
NM_001330504.2:c.739+98C=	NP_001317433.1:n.739+98C=