Canonical Allele Identifier: CA591171
Gene: UBIAD1 HGNC NCBI

Linked Data

dbSNP Id: rs369435530
gnomAD v2: 1-11334159-G-A
gnomAD v3: 1-11274102-G-A
gnomAD v4: 1-11274102-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11274102G>A , CM000663.2:g.11274102G>A GRCh38
NC_000001.10:g.11334159G>A , CM000663.1:g.11334159G>A GRCh37
NC_000001.9:g.11256746G>A NCBI36
NG_009443.1:g.5905G>A
NG_009443.2:g.5905G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.529+42G>A MANE Select ENSP00000366006.5:n.529+42G>A
ENST00000376804.2:c.529+42G>A ENSP00000366000.1:n.529+42G>A
ENST00000376810.5:c.529+42G>A ENSP00000366006.5:n.529+42G>A
ENST00000483738.1:c.127+42G>A ENSP00000473453.1:n.127+42G>A
ENST00000486588.6:c.172+42G>A ENSP00000473612.1:n.172+42G>A
NM_013319.2:c.529+42G>A NP_037451.1:n.529+42G>A
XM_006710590.2:c.529+42G>A XP_006710653.1:n.529+42G>A
XM_011541304.1:c.529+42G>A XP_011539606.1:n.529+42G>A
XR_946616.1:n.863+42G>A
NM_001330349.1:c.529+42G>A NP_001317278.1:n.529+42G>A
NM_001330350.1:c.529+42G>A NP_001317279.1:n.529+42G>A
XR_946616.3:n.863+42G>A
NM_001330349.2:c.529+42G>A NP_001317278.1:n.529+42G>A
NM_001330350.2:c.529+42G>A NP_001317279.1:n.529+42G>A
NM_013319.3:c.529+42G>A MANE Select NP_037451.1:n.529+42G>A