Canonical Allele Identifier: CA591152
Gene: UBIAD1 HGNC NCBI

Linked Data

dbSNP Id: rs779379621
gnomAD v2: 1-11334047-C-A
gnomAD v4: 1-11273990-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273990C>A , CM000663.2:g.11273990C>A GRCh38
NC_000001.10:g.11334047C>A , CM000663.1:g.11334047C>A GRCh37
NC_000001.9:g.11256634C>A NCBI36
NG_009443.1:g.5793C>A
NG_009443.2:g.5793C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.459C>A MANE Select ENSP00000366006.5:p.Ser153=
ENST00000376804.2:c.459C>A ENSP00000366000.1:p.Ser153=
ENST00000376810.5:c.459C>A ENSP00000366006.5:p.Ser153=
ENST00000483738.1:c.57C>A ENSP00000473453.1:p.Ser19=
ENST00000486588.6:c.102C>A ENSP00000473612.1:p.Ser34=
NM_013319.2:c.459C>A NP_037451.1:p.Ser153=
XM_006710590.2:c.459C>A XP_006710653.1:p.Ser153=
XM_011541304.1:c.459C>A XP_011539606.1:p.Ser153=
XR_946616.1:n.793C>A
NM_001330349.1:c.459C>A NP_001317278.1:p.Ser153=
NM_001330350.1:c.459C>A NP_001317279.1:p.Ser153=
XR_946616.3:n.793C>A
NM_001330349.2:c.459C>A NP_001317278.1:p.Ser153=
NM_001330350.2:c.459C>A NP_001317279.1:p.Ser153=
NM_013319.3:c.459C>A MANE Select NP_037451.1:p.Ser153=