Canonical Allele Identifier: CA15085334

Gene: ALG6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63413769A>G , CM000663.2:g.63413769A>G	GRCh38
NC_000001.10:g.63879440A>G , CM000663.1:g.63879440A>G	GRCh37
NC_000001.9:g.63652028A>G	NCBI36
NG_008925.2:g.51180A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_013339.4:c.817-292A>G MANE Select	NP_037471.2:n.817-292A>G
ENST00000263440.6:c.817-292A>G MANE Select	ENSP00000263440.5:n.817-292A>G
NM_013339.3:c.817-292A>G	NP_037471.2:n.817-292A>G
ENST00000263440.4:c.823-292A>G	ENSP00000263440.4:n.823-292A>G
ENST00000371108.8:c.817-292A>G	ENSP00000360149.4:n.817-292A>G
ENST00000465969.5:n.114A>G
ENST00000603108.5:c.826+1704A>G	ENSP00000473934.1:n.826+1704A>G
ENST00000603108.6:c.817-292A>G	ENSP00000473934.2:n.817-292A>G
ENST00000647818.1:c.*123-292A>G	ENSP00000497667.1:n.*123-292A>G
ENST00000648964.1:c.*546-292A>G	ENSP00000497828.1:n.*546-292A>G
ENST00000649570.1:c.*249-302A>G	ENSP00000497742.1:n.*249-302A>G
ENST00000650494.1:c.*119-292A>G	ENSP00000497170.1:n.*119-292A>G