Canonical Allele Identifier: CA338691454

Gene: UBIAD1

Linked Data

• MyVariant Identifiers: chr1:g.11333997T>A (hg19) ; chr1:g.11273940T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11273940T>A , CM000663.2:g.11273940T>A	GRCh38
NC_000001.10:g.11333997T>A , CM000663.1:g.11333997T>A	GRCh37
NC_000001.9:g.11256584T>A	NCBI36
NG_009443.1:g.5743T>A
NG_009443.2:g.5743T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.409T>A MANE Select	ENSP00000366006.5:p.Phe137Ile
ENST00000376804.2:c.409T>A	ENSP00000366000.1:p.Phe137Ile
ENST00000376810.5:c.409T>A	ENSP00000366006.5:p.Phe137Ile
ENST00000483738.1:c.7T>A	ENSP00000473453.1:p.Phe3Ile
ENST00000486588.6:c.52T>A	ENSP00000473612.1:p.Phe18Ile
NM_013319.2:c.409T>A	NP_037451.1:p.Phe137Ile
XM_006710590.2:c.409T>A	XP_006710653.1:p.Phe137Ile
XM_011541304.1:c.409T>A	XP_011539606.1:p.Phe137Ile
XR_946616.1:n.743T>A
NM_001330349.1:c.409T>A	NP_001317278.1:p.Phe137Ile
NM_001330350.1:c.409T>A	NP_001317279.1:p.Phe137Ile
XR_946616.3:n.743T>A
NM_001330349.2:c.409T>A	NP_001317278.1:p.Phe137Ile
NM_001330350.2:c.409T>A	NP_001317279.1:p.Phe137Ile
NM_013319.3:c.409T>A MANE Select	NP_037451.1:p.Phe137Ile