Canonical Allele Identifier: CA2091591709
Gene: ALG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52024678A= , CM000675.2:g.52024678A= GRCh38
NC_000013.10:g.52598814A= , CM000675.1:g.52598814A= GRCh37
NC_000013.9:g.51496815A= NCBI36
NG_028038.1:g.17292A=

Transcript Alleles

HGVS Amino-acid change
ENST00000521508.2:c.948A= MANE Select ENSP00000430236.1:p.Pro316=
ENST00000649340.2:c.948A= ENSP00000497184.2:p.Pro316=
ENST00000649651.2:n.5252A=
ENST00000649708.2:c.275+5535A= ENSP00000497459.2:n.275+5535A=
ENST00000650049.2:c.*56A= ENSP00000497398.2:n.*56A=
ENST00000679359.1:c.*700A= ENSP00000505579.1:n.*700A=
ENST00000679495.1:n.44+12216A=
ENST00000679544.1:c.276-3641A= ENSP00000505560.1:n.276-3641A=
ENST00000680058.1:n.851A=
ENST00000680793.1:n.2200-3641A=
ENST00000680950.1:n.1075A=
ENST00000681047.1:c.*673A= ENSP00000505034.1:n.*673A=
ENST00000681053.1:c.717A= ENSP00000505307.1:p.Pro239=
ENST00000681145.1:c.*1-3644A= ENSP00000505163.1:n.*1-3644A=
ENST00000681226.1:n.396-3641A=
ENST00000519151.1:n.3884A=
ENST00000521508.1:c.948A= ENSP00000430236.1:p.Pro316=
ENST00000523764.1:c.45-3641A= ENSP00000429497.1:n.45-3641A=
NM_001004127.2:c.948A= NP_001004127.2:p.Pro316=
NR_036571.2:n.77-3641A=
NM_001004127.3:c.948A= MANE Select NP_001004127.2:p.Pro316=
NR_036571.3:n.66-3641A=