Canonical Allele Identifier: CA1867298023
Gene: ALG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221571C= , CM000671.2:g.99221571C= GRCh38
NC_000009.11:g.101983853C= , CM000671.1:g.101983853C= GRCh37
NC_000009.10:g.101023674C= NCBI36
NG_008928.1:g.5394G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.324G= MANE Select ENSP00000417764.1:p.Glu108=
ENST00000238477.5:c.324G= ENSP00000432675.2:p.Glu108=
ENST00000476832.1:c.324G= ENSP00000417764.1:p.Glu108=
NM_033087.3:c.324G= NP_149078.1:p.Glu108=
NR_024532.1:n.394G=
NM_033087.4:c.324G= MANE Select NP_149078.1:p.Glu108=
NR_024532.2:n.372G=
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