Canonical Allele Identifier: CA6989768

Gene: ALG11

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52012432A>G , CM000675.2:g.52012432A>G	GRCh38
NC_000013.10:g.52586568A>G , CM000675.1:g.52586568A>G	GRCh37
NC_000013.9:g.51484569A>G	NCBI36
NG_008806.1:g.4063T>C
NG_028038.1:g.5046A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001004127.3:c.14A>G MANE Select	NP_001004127.2:p.Glu5Gly
ENST00000521508.2:c.14A>G MANE Select	ENSP00000430236.1:p.Glu5Gly
NM_001004127.2:c.14A>G	NP_001004127.2:p.Glu5Gly
NR_036571.2:n.46A>G
NR_036571.3:n.35A>G
ENST00000521508.1:c.14A>G	ENSP00000430236.1:p.Glu5Gly
ENST00000523764.1:c.14A>G	ENSP00000429497.1:p.Glu5Gly
ENST00000616513.1:c.14A>G	ENSP00000481922.1:p.Glu5Gly
ENST00000649340.2:c.14A>G	ENSP00000497184.2:p.Glu5Gly
ENST00000649708.2:c.14A>G	ENSP00000497459.2:p.Glu5Gly
ENST00000650049.2:c.14A>G	ENSP00000497398.2:p.Glu5Gly
ENST00000679359.1:c.14A>G	ENSP00000505579.1:p.Glu5Gly
ENST00000679495.1:n.14A>G
ENST00000679544.1:c.14A>G	ENSP00000505560.1:p.Glu5Gly
ENST00000680793.1:n.35A>G
ENST00000680950.1:n.29A>G
ENST00000681047.1:c.14A>G	ENSP00000505034.1:p.Glu5Gly
ENST00000681053.1:c.14A>G	ENSP00000505307.1:p.Glu5Gly
ENST00000681145.1:c.14A>G	ENSP00000505163.1:p.Glu5Gly
ENST00000681226.1:n.22A>G