Canonical Allele Identifier: CA338691892

Gene: UBIAD1

Linked Data

• MyVariant Identifiers: chr1:g.11345782C>A (hg19) ; chr1:g.11285725C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11285725C>A , CM000663.2:g.11285725C>A	GRCh38
NC_000001.10:g.11345782C>A , CM000663.1:g.11345782C>A	GRCh37
NC_000001.9:g.11268369C>A	NCBI36
NG_009443.1:g.17528C>A
NG_009443.2:g.17528C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376810.6:c.611C>A MANE Select	ENSP00000366006.5:p.Ala204Asp
ENST00000376804.2:c.530-9148C>A	ENSP00000366000.1:n.530-9148C>A
ENST00000376810.5:c.611C>A	ENSP00000366006.5:p.Ala204Asp
ENST00000483738.1:c.209C>A	ENSP00000473453.1:p.Ala70Asp
ENST00000486588.6:c.254C>A	ENSP00000473612.1:p.Ala85Asp
NM_013319.2:c.611C>A	NP_037451.1:p.Ala204Asp
XM_006710590.2:c.611C>A	XP_006710653.1:p.Ala204Asp
XM_011541304.1:c.530-9148C>A	XP_011539606.1:n.530-9148C>A
XR_946616.1:n.945C>A
NM_001330349.1:c.611C>A	NP_001317278.1:p.Ala204Asp
NM_001330350.1:c.530-9148C>A	NP_001317279.1:n.530-9148C>A
XR_946616.3:n.945C>A
NM_001330349.2:c.611C>A	NP_001317278.1:p.Ala204Asp
NM_001330350.2:c.530-9148C>A	NP_001317279.1:n.530-9148C>A
NM_013319.3:c.611C>A MANE Select	NP_037451.1:p.Ala204Asp