Canonical Allele Identifier: CA1140568658

Gene: ALG6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63406361T= , CM000663.2:g.63406361T=	GRCh38
NC_000001.10:g.63872032T= , CM000663.1:g.63872032T=	GRCh37
NC_000001.9:g.63644620T=	NCBI36
NG_008925.2:g.43772T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263440.6:c.391T= MANE Select	ENSP00000263440.5:p.Tyr131=
ENST00000603108.6:c.391T=	ENSP00000473934.2:p.Tyr131=
ENST00000647818.1:c.391T=	ENSP00000497667.1:p.Tyr131=
ENST00000648964.1:c.*120T=	ENSP00000497828.1:n.*120T=
ENST00000649570.1:c.391T=	ENSP00000497742.1:p.Tyr131=
ENST00000650494.1:c.391T=	ENSP00000497170.1:p.Tyr131=
ENST00000263440.4:c.391T=	ENSP00000263440.4:p.Tyr131=
ENST00000371108.8:c.391T=	ENSP00000360149.4:p.Tyr131=
ENST00000603108.5:c.391T=	ENSP00000473934.1:p.Tyr131=
NM_013339.3:c.391T=	NP_037471.2:p.Tyr131=
NM_013339.4:c.391T= MANE Select	NP_037471.2:p.Tyr131=