Canonical Allele Identifier: CA338691526
Gene: UBIAD1 HGNC NCBI

Linked Data

gnomAD v4: 1-11273974-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273974G>A , CM000663.2:g.11273974G>A GRCh38
NC_000001.10:g.11334031G>A , CM000663.1:g.11334031G>A GRCh37
NC_000001.9:g.11256618G>A NCBI36
NG_009443.1:g.5777G>A
NG_009443.2:g.5777G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.443G>A MANE Select ENSP00000366006.5:p.Cys148Tyr
ENST00000376804.2:c.443G>A ENSP00000366000.1:p.Cys148Tyr
ENST00000376810.5:c.443G>A ENSP00000366006.5:p.Cys148Tyr
ENST00000483738.1:c.41G>A ENSP00000473453.1:p.Cys14Tyr
ENST00000486588.6:c.86G>A ENSP00000473612.1:p.Cys29Tyr
NM_013319.2:c.443G>A NP_037451.1:p.Cys148Tyr
XM_006710590.2:c.443G>A XP_006710653.1:p.Cys148Tyr
XM_011541304.1:c.443G>A XP_011539606.1:p.Cys148Tyr
XR_946616.1:n.777G>A
NM_001330349.1:c.443G>A NP_001317278.1:p.Cys148Tyr
NM_001330350.1:c.443G>A NP_001317279.1:p.Cys148Tyr
XR_946616.3:n.777G>A
NM_001330349.2:c.443G>A NP_001317278.1:p.Cys148Tyr
NM_001330350.2:c.443G>A NP_001317279.1:p.Cys148Tyr
NM_013319.3:c.443G>A MANE Select NP_037451.1:p.Cys148Tyr