Canonical Allele Identifier: CA1153600549
Gene: UBIAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11285723C= , CM000663.2:g.11285723C= GRCh38
NC_000001.10:g.11345780C= , CM000663.1:g.11345780C= GRCh37
NC_000001.9:g.11268367C= NCBI36
NG_009443.1:g.17526C=
NG_009443.2:g.17526C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376810.6:c.609C= MANE Select ENSP00000366006.5:p.Tyr203=
ENST00000376804.2:c.530-9150C= ENSP00000366000.1:n.530-9150C=
ENST00000376810.5:c.609C= ENSP00000366006.5:p.Tyr203=
ENST00000483738.1:c.207C= ENSP00000473453.1:p.Tyr69=
ENST00000486588.6:c.252C= ENSP00000473612.1:p.Tyr84=
NM_013319.2:c.609C= NP_037451.1:p.Tyr203=
XM_006710590.2:c.609C= XP_006710653.1:p.Tyr203=
XM_011541304.1:c.530-9150C= XP_011539606.1:n.530-9150C=
XR_946616.1:n.943C=
NM_001330349.1:c.609C= NP_001317278.1:p.Tyr203=
NM_001330350.1:c.530-9150C= NP_001317279.1:n.530-9150C=
XR_946616.3:n.943C=
NM_001330349.2:c.609C= NP_001317278.1:p.Tyr203=
NM_001330350.2:c.530-9150C= NP_001317279.1:n.530-9150C=
NM_013319.3:c.609C= MANE Select NP_037451.1:p.Tyr203=