Canonical Allele Identifier: CA591156

Gene: UBIAD1

Linked Data

• dbSNP Id: rs770846493
• ExAC: 1:11334075 A / T
• gnomAD v2: 1-11334075-A-T
• gnomAD v4: 1-11274018-A-T
• MyVariant Identifiers: chr1:g.11334075A>T (hg19) ; chr1:g.11274018A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11274018A>T , CM000663.2:g.11274018A>T	GRCh38
NC_000001.10:g.11334075A>T , CM000663.1:g.11334075A>T	GRCh37
NC_000001.9:g.11256662A>T	NCBI36
NG_009443.1:g.5821A>T
NG_009443.2:g.5821A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.487A>T MANE Select	ENSP00000366006.5:p.Ile163Phe
ENST00000376804.2:c.487A>T	ENSP00000366000.1:p.Ile163Phe
ENST00000376810.5:c.487A>T	ENSP00000366006.5:p.Ile163Phe
ENST00000483738.1:c.85A>T	ENSP00000473453.1:p.Ile29Phe
ENST00000486588.6:c.130A>T	ENSP00000473612.1:p.Ile44Phe
NM_013319.2:c.487A>T	NP_037451.1:p.Ile163Phe
XM_006710590.2:c.487A>T	XP_006710653.1:p.Ile163Phe
XM_011541304.1:c.487A>T	XP_011539606.1:p.Ile163Phe
XR_946616.1:n.821A>T
NM_001330349.1:c.487A>T	NP_001317278.1:p.Ile163Phe
NM_001330350.1:c.487A>T	NP_001317279.1:p.Ile163Phe
XR_946616.3:n.821A>T
NM_001330349.2:c.487A>T	NP_001317278.1:p.Ile163Phe
NM_001330350.2:c.487A>T	NP_001317279.1:p.Ile163Phe
NM_013319.3:c.487A>T MANE Select	NP_037451.1:p.Ile163Phe