Canonical Allele Identifier: CA340636341
Gene: ALG6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63414065A>T , CM000663.2:g.63414065A>T GRCh38
NC_000001.10:g.63879736A>T , CM000663.1:g.63879736A>T GRCh37
NC_000001.9:g.63652324A>T NCBI36
NG_008925.2:g.51476A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263440.6:c.821A>T MANE Select ENSP00000263440.5:p.Lys274Ile
ENST00000603108.6:c.821A>T ENSP00000473934.2:p.Lys274Ile
ENST00000647818.1:c.*127A>T ENSP00000497667.1:n.*127A>T
ENST00000648964.1:c.*550A>T ENSP00000497828.1:n.*550A>T
ENST00000649570.1:c.*249-6A>T ENSP00000497742.1:n.*249-6A>T
ENST00000650494.1:c.*123A>T ENSP00000497170.1:n.*123A>T
ENST00000263440.4:c.827A>T ENSP00000263440.4:p.Lys276Ile
ENST00000371108.8:c.821A>T ENSP00000360149.4:p.Lys274Ile
ENST00000465969.5:n.410A>T
ENST00000603108.5:c.827-1808A>T ENSP00000473934.1:n.827-1808A>T
NM_013339.3:c.821A>T NP_037471.2:p.Lys274Ile
NM_013339.4:c.821A>T MANE Select NP_037471.2:p.Lys274Ile