Canonical Allele Identifier: CA591147
Gene: UBIAD1 HGNC NCBI

Linked Data

dbSNP Id: rs761216594
gnomAD v2: 1-11334035-C-T
gnomAD v3: 1-11273978-C-T
gnomAD v4: 1-11273978-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273978C>T , CM000663.2:g.11273978C>T GRCh38
NC_000001.10:g.11334035C>T , CM000663.1:g.11334035C>T GRCh37
NC_000001.9:g.11256622C>T NCBI36
NG_009443.1:g.5781C>T
NG_009443.2:g.5781C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.447C>T MANE Select ENSP00000366006.5:p.Leu149=
ENST00000376804.2:c.447C>T ENSP00000366000.1:p.Leu149=
ENST00000376810.5:c.447C>T ENSP00000366006.5:p.Leu149=
ENST00000483738.1:c.45C>T ENSP00000473453.1:p.Leu15=
ENST00000486588.6:c.90C>T ENSP00000473612.1:p.Leu30=
NM_013319.2:c.447C>T NP_037451.1:p.Leu149=
XM_006710590.2:c.447C>T XP_006710653.1:p.Leu149=
XM_011541304.1:c.447C>T XP_011539606.1:p.Leu149=
XR_946616.1:n.781C>T
NM_001330349.1:c.447C>T NP_001317278.1:p.Leu149=
NM_001330350.1:c.447C>T NP_001317279.1:p.Leu149=
XR_946616.3:n.781C>T
NM_001330349.2:c.447C>T NP_001317278.1:p.Leu149=
NM_001330350.2:c.447C>T NP_001317279.1:p.Leu149=
NM_013319.3:c.447C>T MANE Select NP_037451.1:p.Leu149=