Canonical Allele Identifier: CA1153587656
Gene: UBIAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273980A= , CM000663.2:g.11273980A= GRCh38
NC_000001.10:g.11334037A= , CM000663.1:g.11334037A= GRCh37
NC_000001.9:g.11256624A= NCBI36
NG_009443.1:g.5783A=
NG_009443.2:g.5783A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.449A= MANE Select ENSP00000366006.5:p.Tyr150=
ENST00000376804.2:c.449A= ENSP00000366000.1:p.Tyr150=
ENST00000376810.5:c.449A= ENSP00000366006.5:p.Tyr150=
ENST00000483738.1:c.47A= ENSP00000473453.1:p.Tyr16=
ENST00000486588.6:c.92A= ENSP00000473612.1:p.Tyr31=
NM_013319.2:c.449A= NP_037451.1:p.Tyr150=
XM_006710590.2:c.449A= XP_006710653.1:p.Tyr150=
XM_011541304.1:c.449A= XP_011539606.1:p.Tyr150=
XR_946616.1:n.783A=
NM_001330349.1:c.449A= NP_001317278.1:p.Tyr150=
NM_001330350.1:c.449A= NP_001317279.1:p.Tyr150=
XR_946616.3:n.783A=
NM_001330349.2:c.449A= NP_001317278.1:p.Tyr150=
NM_001330350.2:c.449A= NP_001317279.1:p.Tyr150=
NM_013319.3:c.449A= MANE Select NP_037451.1:p.Tyr150=