Canonical Allele Identifier: CA1867298187
Gene: ALG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221632A= , CM000671.2:g.99221632A= GRCh38
NC_000009.11:g.101983914A= , CM000671.1:g.101983914A= GRCh37
NC_000009.10:g.101023735A= NCBI36
NG_008928.1:g.5333T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.263T= MANE Select ENSP00000417764.1:p.Val88=
ENST00000238477.5:c.263T= ENSP00000432675.2:p.Val88=
ENST00000476832.1:c.263T= ENSP00000417764.1:p.Val88=
NM_033087.3:c.263T= NP_149078.1:p.Val88=
NR_024532.1:n.333T=
NM_033087.4:c.263T= MANE Select NP_149078.1:p.Val88=
NR_024532.2:n.311T=
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