Canonical Allele Identifier: CA2091591690
Gene: ALG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52024665A= , CM000675.2:g.52024665A= GRCh38
NC_000013.10:g.52598801A= , CM000675.1:g.52598801A= GRCh37
NC_000013.9:g.51496802A= NCBI36
NG_028038.1:g.17279A=

Transcript Alleles

HGVS Amino-acid change
ENST00000521508.2:c.935A= MANE Select ENSP00000430236.1:p.Glu312=
ENST00000649340.2:c.935A= ENSP00000497184.2:p.Glu312=
ENST00000649651.2:n.5239A=
ENST00000649708.2:c.275+5522A= ENSP00000497459.2:n.275+5522A=
ENST00000650049.2:c.*43A= ENSP00000497398.2:n.*43A=
ENST00000679359.1:c.*687A= ENSP00000505579.1:n.*687A=
ENST00000679495.1:n.44+12203A=
ENST00000679544.1:c.276-3654A= ENSP00000505560.1:n.276-3654A=
ENST00000680058.1:n.838A=
ENST00000680793.1:n.2200-3654A=
ENST00000680950.1:n.1062A=
ENST00000681047.1:c.*660A= ENSP00000505034.1:n.*660A=
ENST00000681053.1:c.704A= ENSP00000505307.1:p.Glu235=
ENST00000681145.1:c.*1-3657A= ENSP00000505163.1:n.*1-3657A=
ENST00000681226.1:n.396-3654A=
ENST00000519151.1:n.3871A=
ENST00000521508.1:c.935A= ENSP00000430236.1:p.Glu312=
ENST00000523764.1:c.45-3654A= ENSP00000429497.1:n.45-3654A=
NM_001004127.2:c.935A= NP_001004127.2:p.Glu312=
NR_036571.2:n.77-3654A=
NM_001004127.3:c.935A= MANE Select NP_001004127.2:p.Glu312=
NR_036571.3:n.66-3654A=