Canonical Allele Identifier: CA2203687524
Gene: ALG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5082569C= , CM000678.2:g.5082569C= GRCh38
NC_000016.9:g.5132570C= , CM000678.1:g.5132570C= GRCh37
NC_000016.8:g.5072571C= NCBI36
NG_009202.1:g.15761C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000592793.6:n.3219C=
ENST00000682020.1:c.489C= ENSP00000508075.1:p.Asp163=
ENST00000682206.1:c.*178C= ENSP00000508285.1:n.*178C=
ENST00000682314.1:n.1131C=
ENST00000682327.1:c.555C= ENSP00000507058.1:p.Asp185=
ENST00000682349.1:n.3225C=
ENST00000682703.1:n.4051C=
ENST00000682797.1:c.*175C= ENSP00000507582.1:n.*175C=
ENST00000682985.1:c.594C= ENSP00000507598.1:p.Asp198=
ENST00000683433.1:c.342C= ENSP00000507463.1:p.Asp114=
ENST00000683685.1:n.1957C=
ENST00000683710.1:c.*1050C= ENSP00000506785.1:n.*1050C=
ENST00000683739.1:c.750C= ENSP00000507002.1:p.Asp250=
ENST00000683772.1:n.1127C=
ENST00000684008.1:c.1021C= ENSP00000507962.1:n.1021C=
ENST00000684190.1:c.1044C= ENSP00000507554.1:p.Asp348=
ENST00000684335.1:c.972C= ENSP00000508112.1:p.Asp324=
ENST00000262374.10:c.1083C= MANE Select ENSP00000262374.5:p.Asp361=
ENST00000650085.1:n.1907C=
ENST00000262374.9:c.1083C= ENSP00000262374.4:p.Asp361=
ENST00000544428.1:c.750C= ENSP00000440019.1:p.Asp250=
ENST00000588623.5:c.750C= ENSP00000468118.1:p.Asp250=
ENST00000591822.5:c.*984C= ENSP00000467865.1:n.*984C=
NM_019109.4:c.1083C= NP_061982.3:p.Asp361=
XM_011522565.1:c.750C= XP_011520867.1:p.Asp250=
NM_001330504.1:c.750C= NP_001317433.1:p.Asp250=
XM_017023457.2:c.1044C= XP_016878946.1:p.Asp348=
XM_017023458.1:c.750C= XP_016878947.1:p.Asp250=
XR_932882.3:n.1112C=
NM_019109.5:c.1083C= MANE Select NP_061982.3:p.Asp361=
NM_001330504.2:c.750C= NP_001317433.1:p.Asp250=