Canonical Allele Identifier: CA2643254332

Gene: UBIAD1

Linked Data

• gnomAD v4: 1-11287129-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11287129A>G , CM000663.2:g.11287129A>G	GRCh38
NC_000001.10:g.11347186A>G , CM000663.1:g.11347186A>G	GRCh37
NC_000001.9:g.11269773A>G	NCBI36
NG_009443.1:g.18932A>G
NG_009443.2:g.18932A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.*998A>G MANE Select	ENSP00000366006.5:n.*998A>G
ENST00000376804.2:c.530-7744A>G	ENSP00000366000.1:n.530-7744A>G
ENST00000376810.5:c.*998A>G	ENSP00000366006.5:n.*998A>G
ENST00000483738.1:c.216+1397A>G	ENSP00000473453.1:n.216+1397A>G
ENST00000486588.6:c.261+1397A>G	ENSP00000473612.1:n.261+1397A>G
NM_013319.2:c.*998A>G	NP_037451.1:n.*998A>G
XM_006710590.2:c.618+1397A>G	XP_006710653.1:n.618+1397A>G
XM_011541304.1:c.530-7744A>G	XP_011539606.1:n.530-7744A>G
XR_946616.1:n.952+1397A>G
NM_001330349.1:c.618+1397A>G	NP_001317278.1:n.618+1397A>G
NM_001330350.1:c.530-7744A>G	NP_001317279.1:n.530-7744A>G
XR_946616.3:n.952+1397A>G
NM_001330349.2:c.618+1397A>G	NP_001317278.1:n.618+1397A>G
NM_001330350.2:c.530-7744A>G	NP_001317279.1:n.530-7744A>G
NM_013319.3:c.*998A>G MANE Select	NP_037451.1:n.*998A>G