Canonical Allele Identifier: CA1141649095
Gene: UBIAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273964T= , CM000663.2:g.11273964T= GRCh38
NC_000001.10:g.11334021T= , CM000663.1:g.11334021T= GRCh37
NC_000001.9:g.11256608T= NCBI36
NG_009443.1:g.5767T=
NG_009443.2:g.5767T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.433T= MANE Select ENSP00000366006.5:p.Cys145=
ENST00000376804.2:c.433T= ENSP00000366000.1:p.Cys145=
ENST00000376810.5:c.433T= ENSP00000366006.5:p.Cys145=
ENST00000483738.1:c.31T= ENSP00000473453.1:p.Cys11=
ENST00000486588.6:c.76T= ENSP00000473612.1:p.Cys26=
NM_013319.2:c.433T= NP_037451.1:p.Cys145=
XM_006710590.2:c.433T= XP_006710653.1:p.Cys145=
XM_011541304.1:c.433T= XP_011539606.1:p.Cys145=
XR_946616.1:n.767T=
NM_001330349.1:c.433T= NP_001317278.1:p.Cys145=
NM_001330350.1:c.433T= NP_001317279.1:p.Cys145=
XR_946616.3:n.767T=
NM_001330349.2:c.433T= NP_001317278.1:p.Cys145=
NM_001330350.2:c.433T= NP_001317279.1:p.Cys145=
NM_013319.3:c.433T= MANE Select NP_037451.1:p.Cys145=