Canonical Allele Identifier: CA18415492

Gene: UBIAD1

Linked Data

• dbSNP Id: rs138952691
• MyVariant Identifiers: chr1:g.11334021T>G (hg19) ; chr1:g.11273964T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11273964T>G , CM000663.2:g.11273964T>G	GRCh38
NC_000001.10:g.11334021T>G , CM000663.1:g.11334021T>G	GRCh37
NC_000001.9:g.11256608T>G	NCBI36
NG_009443.1:g.5767T>G
NG_009443.2:g.5767T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.433T>G MANE Select	ENSP00000366006.5:p.Cys145Gly
ENST00000376804.2:c.433T>G	ENSP00000366000.1:p.Cys145Gly
ENST00000376810.5:c.433T>G	ENSP00000366006.5:p.Cys145Gly
ENST00000483738.1:c.31T>G	ENSP00000473453.1:p.Cys11Gly
ENST00000486588.6:c.76T>G	ENSP00000473612.1:p.Cys26Gly
NM_013319.2:c.433T>G	NP_037451.1:p.Cys145Gly
XM_006710590.2:c.433T>G	XP_006710653.1:p.Cys145Gly
XM_011541304.1:c.433T>G	XP_011539606.1:p.Cys145Gly
XR_946616.1:n.767T>G
NM_001330349.1:c.433T>G	NP_001317278.1:p.Cys145Gly
NM_001330350.1:c.433T>G	NP_001317279.1:p.Cys145Gly
XR_946616.3:n.767T>G
NM_001330349.2:c.433T>G	NP_001317278.1:p.Cys145Gly
NM_001330350.2:c.433T>G	NP_001317279.1:p.Cys145Gly
NM_013319.3:c.433T>G MANE Select	NP_037451.1:p.Cys145Gly