Canonical Allele Identifier: CA1867298035
Gene: ALG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221576C= , CM000671.2:g.99221576C= GRCh38
NC_000009.11:g.101983858C= , CM000671.1:g.101983858C= GRCh37
NC_000009.10:g.101023679C= NCBI36
NG_008928.1:g.5389G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.319G= MANE Select ENSP00000417764.1:p.Glu107=
ENST00000238477.5:c.319G= ENSP00000432675.2:p.Glu107=
ENST00000476832.1:c.319G= ENSP00000417764.1:p.Glu107=
NM_033087.3:c.319G= NP_149078.1:p.Glu107=
NR_024532.1:n.389G=
NM_033087.4:c.319G= MANE Select NP_149078.1:p.Glu107=
NR_024532.2:n.367G=