Canonical Allele Identifier: CA1149062316
Gene: UBIAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11274041C= , CM000663.2:g.11274041C= GRCh38
NC_000001.10:g.11334098C= , CM000663.1:g.11334098C= GRCh37
NC_000001.9:g.11256685C= NCBI36
NG_009443.1:g.5844C=
NG_009443.2:g.5844C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.510C= MANE Select ENSP00000366006.5:p.Gly170=
ENST00000376804.2:c.510C= ENSP00000366000.1:p.Gly170=
ENST00000376810.5:c.510C= ENSP00000366006.5:p.Gly170=
ENST00000483738.1:c.108C= ENSP00000473453.1:p.Gly36=
ENST00000486588.6:c.153C= ENSP00000473612.1:p.Gly51=
NM_013319.2:c.510C= NP_037451.1:p.Gly170=
XM_006710590.2:c.510C= XP_006710653.1:p.Gly170=
XM_011541304.1:c.510C= XP_011539606.1:p.Gly170=
XR_946616.1:n.844C=
NM_001330349.1:c.510C= NP_001317278.1:p.Gly170=
NM_001330350.1:c.510C= NP_001317279.1:p.Gly170=
XR_946616.3:n.844C=
NM_001330349.2:c.510C= NP_001317278.1:p.Gly170=
NM_001330350.2:c.510C= NP_001317279.1:p.Gly170=
NM_013319.3:c.510C= MANE Select NP_037451.1:p.Gly170=