Canonical Allele Identifier: CA2643254335
Gene: UBIAD1 HGNC NCBI

Linked Data

gnomAD v4: 1-11287131-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11287131C>A , CM000663.2:g.11287131C>A GRCh38
NC_000001.10:g.11347188C>A , CM000663.1:g.11347188C>A GRCh37
NC_000001.9:g.11269775C>A NCBI36
NG_009443.1:g.18934C>A
NG_009443.2:g.18934C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.*1000C>A MANE Select ENSP00000366006.5:n.*1000C>A
ENST00000376804.2:c.530-7742C>A ENSP00000366000.1:n.530-7742C>A
ENST00000376810.5:c.*1000C>A ENSP00000366006.5:n.*1000C>A
ENST00000483738.1:c.216+1399C>A ENSP00000473453.1:n.216+1399C>A
ENST00000486588.6:c.261+1399C>A ENSP00000473612.1:n.261+1399C>A
NM_013319.2:c.*1000C>A NP_037451.1:n.*1000C>A
XM_006710590.2:c.618+1399C>A XP_006710653.1:n.618+1399C>A
XM_011541304.1:c.530-7742C>A XP_011539606.1:n.530-7742C>A
XR_946616.1:n.952+1399C>A
NM_001330349.1:c.618+1399C>A NP_001317278.1:n.618+1399C>A
NM_001330350.1:c.530-7742C>A NP_001317279.1:n.530-7742C>A
XR_946616.3:n.952+1399C>A
NM_001330349.2:c.618+1399C>A NP_001317278.1:n.618+1399C>A
NM_001330350.2:c.530-7742C>A NP_001317279.1:n.530-7742C>A
NM_013319.3:c.*1000C>A MANE Select NP_037451.1:n.*1000C>A