Canonical Allele Identifier: CA1171486662

Gene: ALG6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63415886T= , CM000663.2:g.63415886T=	GRCh38
NC_000001.10:g.63881557T= , CM000663.1:g.63881557T=	GRCh37
NC_000001.9:g.63654145T=	NCBI36
NG_008925.2:g.53297T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263440.6:c.916T= MANE Select	ENSP00000263440.5:p.Phe306=
ENST00000603108.6:c.*65T=	ENSP00000473934.2:n.*65T=
ENST00000647818.1:c.*222T=	ENSP00000497667.1:n.*222T=
ENST00000648964.1:c.*645T=	ENSP00000497828.1:n.*645T=
ENST00000649570.1:c.*338T=	ENSP00000497742.1:n.*338T=
ENST00000650494.1:c.*273T=	ENSP00000497170.1:n.*273T=
ENST00000263440.4:c.922T=	ENSP00000263440.4:p.Phe308=
ENST00000371108.8:c.916T=	ENSP00000360149.4:p.Phe306=
ENST00000465969.5:n.505T=
ENST00000603108.5:c.840T=	ENSP00000473934.1:p.Arg280=
NM_013339.3:c.916T=	NP_037471.2:p.Phe306=
NM_013339.4:c.916T= MANE Select	NP_037471.2:p.Phe306=