Canonical Allele Identifier: CA2203685642
Gene: ALG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5080957C= , CM000678.2:g.5080957C= GRCh38
NC_000016.9:g.5130958C= , CM000678.1:g.5130958C= GRCh37
NC_000016.8:g.5070959C= NCBI36
NG_009202.1:g.14149C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000592793.6:n.3109C=
ENST00000682020.1:c.379C= ENSP00000508075.1:p.Leu127=
ENST00000682206.1:c.*65C= ENSP00000508285.1:n.*65C=
ENST00000682314.1:n.1021C=
ENST00000682327.1:c.445C= ENSP00000507058.1:p.Leu149=
ENST00000682349.1:n.3115C=
ENST00000682703.1:n.3941C=
ENST00000682797.1:c.*65C= ENSP00000507582.1:n.*65C=
ENST00000682985.1:c.484C= ENSP00000507598.1:p.Leu162=
ENST00000683433.1:c.229C= ENSP00000507463.1:p.Leu77=
ENST00000683685.1:n.1847C=
ENST00000683710.1:c.*940C= ENSP00000506785.1:n.*940C=
ENST00000683739.1:c.640C= ENSP00000507002.1:p.Leu214=
ENST00000683772.1:n.1017C=
ENST00000684008.1:c.911C= ENSP00000507962.1:n.911C=
ENST00000684190.1:c.934C= ENSP00000507554.1:p.Leu312=
ENST00000684335.1:c.961+1150C= ENSP00000508112.1:n.961+1150C=
ENST00000262374.10:c.973C= MANE Select ENSP00000262374.5:p.Leu325=
ENST00000650085.1:n.1797C=
ENST00000262374.9:c.973C= ENSP00000262374.4:p.Leu325=
ENST00000544428.1:c.640C= ENSP00000440019.1:p.Leu214=
ENST00000588623.5:c.640C= ENSP00000468118.1:p.Leu214=
ENST00000591822.5:c.*874C= ENSP00000467865.1:n.*874C=
NM_019109.4:c.973C= NP_061982.3:p.Leu325=
XM_011522565.1:c.640C= XP_011520867.1:p.Leu214=
XR_932882.1:n.1018C=
NM_001330504.1:c.640C= NP_001317433.1:p.Leu214=
XM_017023457.2:c.934C= XP_016878946.1:p.Leu312=
XM_017023458.1:c.640C= XP_016878947.1:p.Leu214=
XR_932882.3:n.1002C=
NM_019109.5:c.973C= MANE Select NP_061982.3:p.Leu325=
NM_001330504.2:c.640C= NP_001317433.1:p.Leu214=