Canonical Allele Identifier: CA1153587623
Gene: UBIAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273956G= , CM000663.2:g.11273956G= GRCh38
NC_000001.10:g.11334013G= , CM000663.1:g.11334013G= GRCh37
NC_000001.9:g.11256600G= NCBI36
NG_009443.1:g.5759G=
NG_009443.2:g.5759G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.425G= MANE Select ENSP00000366006.5:p.Gly142=
ENST00000376804.2:c.425G= ENSP00000366000.1:p.Gly142=
ENST00000376810.5:c.425G= ENSP00000366006.5:p.Gly142=
ENST00000483738.1:c.23G= ENSP00000473453.1:p.Gly8=
ENST00000486588.6:c.68G= ENSP00000473612.1:p.Gly23=
NM_013319.2:c.425G= NP_037451.1:p.Gly142=
XM_006710590.2:c.425G= XP_006710653.1:p.Gly142=
XM_011541304.1:c.425G= XP_011539606.1:p.Gly142=
XR_946616.1:n.759G=
NM_001330349.1:c.425G= NP_001317278.1:p.Gly142=
NM_001330350.1:c.425G= NP_001317279.1:p.Gly142=
XR_946616.3:n.759G=
NM_001330349.2:c.425G= NP_001317278.1:p.Gly142=
NM_001330350.2:c.425G= NP_001317279.1:p.Gly142=
NM_013319.3:c.425G= MANE Select NP_037451.1:p.Gly142=