Canonical Allele Identifier: CA1171485569

Gene: ALG6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63414049A= , CM000663.2:g.63414049A=	GRCh38
NC_000001.10:g.63879720A= , CM000663.1:g.63879720A=	GRCh37
NC_000001.9:g.63652308A=	NCBI36
NG_008925.2:g.51460A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263440.6:c.817-12A= MANE Select	ENSP00000263440.5:n.817-12A=
ENST00000603108.6:c.817-12A=	ENSP00000473934.2:n.817-12A=
ENST00000647818.1:c.*123-12A=	ENSP00000497667.1:n.*123-12A=
ENST00000648964.1:c.*546-12A=	ENSP00000497828.1:n.*546-12A=
ENST00000649570.1:c.*249-22A=	ENSP00000497742.1:n.*249-22A=
ENST00000650494.1:c.*119-12A=	ENSP00000497170.1:n.*119-12A=
ENST00000263440.4:c.823-12A=	ENSP00000263440.4:n.823-12A=
ENST00000371108.8:c.817-12A=	ENSP00000360149.4:n.817-12A=
ENST00000465969.5:n.394A=
ENST00000603108.5:c.827-1824A=	ENSP00000473934.1:n.827-1824A=
NM_013339.3:c.817-12A=	NP_037471.2:n.817-12A=
NM_013339.4:c.817-12A= MANE Select	NP_037471.2:n.817-12A=