Canonical Allele Identifier: CA2203687526
Gene: ALG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5082570C= , CM000678.2:g.5082570C= GRCh38
NC_000016.9:g.5132571C= , CM000678.1:g.5132571C= GRCh37
NC_000016.8:g.5072572C= NCBI36
NG_009202.1:g.15762C=

Transcript Alleles

HGVS Amino-acid change
ENST00000592793.6:n.3220C=
ENST00000682020.1:c.490C= ENSP00000508075.1:p.Leu164=
ENST00000682206.1:c.*179C= ENSP00000508285.1:n.*179C=
ENST00000682314.1:n.1132C=
ENST00000682327.1:c.556C= ENSP00000507058.1:p.Leu186=
ENST00000682349.1:n.3226C=
ENST00000682703.1:n.4052C=
ENST00000682797.1:c.*176C= ENSP00000507582.1:n.*176C=
ENST00000682985.1:c.595C= ENSP00000507598.1:p.Leu199=
ENST00000683433.1:c.343C= ENSP00000507463.1:p.Leu115=
ENST00000683685.1:n.1958C=
ENST00000683710.1:c.*1051C= ENSP00000506785.1:n.*1051C=
ENST00000683739.1:c.751C= ENSP00000507002.1:p.Leu251=
ENST00000683772.1:n.1128C=
ENST00000684008.1:c.1022C= ENSP00000507962.1:n.1022C=
ENST00000684190.1:c.1045C= ENSP00000507554.1:p.Leu349=
ENST00000684335.1:c.973C= ENSP00000508112.1:p.Leu325=
ENST00000262374.10:c.1084C= MANE Select ENSP00000262374.5:p.Leu362=
ENST00000650085.1:n.1908C=
ENST00000262374.9:c.1084C= ENSP00000262374.4:p.Leu362=
ENST00000544428.1:c.751C= ENSP00000440019.1:p.Leu251=
ENST00000588623.5:c.751C= ENSP00000468118.1:p.Leu251=
ENST00000591822.5:c.*985C= ENSP00000467865.1:n.*985C=
NM_019109.4:c.1084C= NP_061982.3:p.Leu362=
XM_011522565.1:c.751C= XP_011520867.1:p.Leu251=
NM_001330504.1:c.751C= NP_001317433.1:p.Leu251=
XM_017023457.2:c.1045C= XP_016878946.1:p.Leu349=
XM_017023458.1:c.751C= XP_016878947.1:p.Leu251=
XR_932882.3:n.1113C=
NM_019109.5:c.1084C= MANE Select NP_061982.3:p.Leu362=
NM_001330504.2:c.751C= NP_001317433.1:p.Leu251=