Canonical Allele Identifier: CA2091584827

Gene: ALG11 UTP14C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52028201A= , CM000675.2:g.52028201A=	GRCh38
NC_000013.10:g.52602337A= , CM000675.1:g.52602337A=	GRCh37
NC_000013.9:g.51500338A=	NCBI36
NG_028038.1:g.20815A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521508.2:c.1208-118A= (ALG11) MANE Select	ENSP00000430236.1:n.1208-118A=
ENST00000649340.2:c.1208-121A= (ALG11)	ENSP00000497184.2:n.1208-121A=
ENST00000649651.2:n.5512-118A= (ALG11)
ENST00000649708.2:c.275+9058A= (ALG11)	ENSP00000497459.2:n.275+9058A=
ENST00000650049.2:c.*316-118A= (ALG11)	ENSP00000497398.2:n.*316-118A=
ENST00000679359.1:c.*960-118A= (ALG11)	ENSP00000505579.1:n.*960-118A=
ENST00000679495.1:n.44+15739A= (ALG11)
ENST00000679544.1:c.276-118A= (ALG11)	ENSP00000505560.1:n.276-118A=
ENST00000680058.1:n.1111-118A= (ALG11)
ENST00000680793.1:n.2200-118A= (ALG11)
ENST00000680950.1:n.1335-118A= (ALG11)
ENST00000681047.1:c.*933-118A= (ALG11)	ENSP00000505034.1:n.*933-118A=
ENST00000681053.1:c.977-118A= (ALG11)	ENSP00000505307.1:n.977-118A=
ENST00000681145.1:c.*1-121A= (ALG11)	ENSP00000505163.1:n.*1-121A=
ENST00000681226.1:n.396-118A= (ALG11)
ENST00000519151.1:n.4144-118A= (ALG11)
ENST00000521508.1:c.1208-118A= (ALG11)	ENSP00000430236.1:n.1208-118A=
ENST00000521776.2:c.-486-118A= (UTP14C) MANE Select	ENSP00000428619.1:n.-486-118A=
ENST00000523764.1:c.45-118A= (ALG11)	ENSP00000429497.1:n.45-118A=
NM_001004127.2:c.1208-118A= (ALG11)	NP_001004127.2:n.1208-118A=
NM_021645.5:c.-486-118A= (UTP14C)	NP_067677.4:n.-486-118A=
NR_036571.2:n.77-118A= (ALG11)
NM_001004127.3:c.1208-118A= (ALG11) MANE Select	NP_001004127.2:n.1208-118A=
NM_021645.6:c.-486-118A= (UTP14C) MANE Select	NP_067677.4:n.-486-118A=
NR_036571.3:n.66-118A= (ALG11)