Canonical Allele Identifier: CA2657454443
Gene: ALG12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49913617del , CM000684.2:g.49913617del GRCh38
NC_000022.10:g.50307265del , CM000684.1:g.50307265del GRCh37
NC_000022.9:g.48693269del NCBI36
NG_008927.1:g.9843del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330817.11:c.150del MANE Select ENSP00000333813.5:p.Asp51ThrfsTer23
ENST00000330817.10:c.150del ENSP00000333813.5:p.Asp51ThrfsTer23
NM_024105.3:c.150del NP_077010.1:p.Asp51ThrfsTer23
XM_011530369.1:c.150del XP_011528671.1:p.Asp51ThrfsTer23
XM_011530370.1:c.150del XP_011528672.1:p.Asp51ThrfsTer23
XM_011530371.1:c.150del XP_011528673.1:p.Asp51ThrfsTer23
XM_011530371.2:c.150del XP_011528673.1:p.Asp51ThrfsTer23
XM_017028936.1:c.150del XP_016884425.1:p.Asp51ThrfsTer23
XM_017028937.1:c.150del XP_016884426.1:p.Asp51ThrfsTer23
NM_024105.4:c.150del MANE Select NP_077010.1:p.Asp51ThrfsTer23