Canonical Allele Identifier: CA394678416
Community Standard Title: NM_019109.5(ALG1):c.11C>G (p.Ser4Ter)
Gene: ALG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5071860C>G , CM000678.2:g.5071860C>G GRCh38
NC_000016.9:g.5121861C>G , CM000678.1:g.5121861C>G GRCh37
NC_000016.8:g.5061862C>G NCBI36
NG_009202.1:g.5052C>G

Transcript Alleles

HGVS Amino-acid Change
NM_019109.5:c.11C>G MANE Select NP_061982.3:p.Ser4Ter
ENST00000262374.10:c.11C>G MANE Select ENSP00000262374.5:p.Ser4Ter
NM_019109.4:c.11C>G NP_061982.3:p.Ser4Ter
ENST00000262374.9:c.11C>G ENSP00000262374.4:p.Ser4Ter
ENST00000586840.1:c.11C>G ENSP00000467538.1:p.Ser4Ter
ENST00000588623.5:c.-125-1091C>G ENSP00000468118.1:n.-125-1091C>G
ENST00000591822.5:c.11C>G ENSP00000467865.1:p.Ser4Ter
ENST00000592793.5:n.18C>G
ENST00000592793.6:n.18C>G
ENST00000650085.1:n.1013-1091C>G
ENST00000682020.1:c.-55-5585C>G ENSP00000508075.1:n.-55-5585C>G
ENST00000682206.1:c.11C>G ENSP00000508285.1:p.Ser4Ter
ENST00000682314.1:n.55C>G
ENST00000682327.1:c.-99-3528C>G ENSP00000507058.1:n.-99-3528C>G
ENST00000682349.1:n.18C>G
ENST00000682703.1:n.18C>G
ENST00000682797.1:c.11C>G ENSP00000507582.1:p.Ser4Ter
ENST00000682985.1:c.-99-3528C>G ENSP00000507598.1:n.-99-3528C>G
ENST00000683433.1:c.-55-5585C>G ENSP00000507463.1:n.-55-5585C>G
ENST00000683685.1:n.55C>G
ENST00000683710.1:c.11C>G ENSP00000506785.1:p.Ser4Ter
ENST00000683772.1:n.55C>G
ENST00000684008.1:c.11C>G ENSP00000507962.1:p.Ser4Ter
ENST00000684190.1:c.11C>G ENSP00000507554.1:p.Ser4Ter
ENST00000684335.1:c.11C>G ENSP00000508112.1:p.Ser4Ter
XM_017023457.2:c.11C>G XP_016878946.1:p.Ser4Ter
XM_017023458.1:c.-479C>G XP_016878947.1:n.-479C>G
XR_932882.1:n.52C>G
XR_932882.3:n.36C>G