Canonical Allele Identifier: CA18415504

Gene: UBIAD1

Linked Data

• dbSNP Id: rs763246532
• gnomAD v4: 1-11274103-T-G
• MyVariant Identifiers: chr1:g.11334160T>G (hg19) ; chr1:g.11274103T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11274103T>G , CM000663.2:g.11274103T>G	GRCh38
NC_000001.10:g.11334160T>G , CM000663.1:g.11334160T>G	GRCh37
NC_000001.9:g.11256747T>G	NCBI36
NG_009443.1:g.5906T>G
NG_009443.2:g.5906T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.529+43T>G MANE Select	ENSP00000366006.5:n.529+43T>G
ENST00000376804.2:c.529+43T>G	ENSP00000366000.1:n.529+43T>G
ENST00000376810.5:c.529+43T>G	ENSP00000366006.5:n.529+43T>G
ENST00000483738.1:c.127+43T>G	ENSP00000473453.1:n.127+43T>G
ENST00000486588.6:c.172+43T>G	ENSP00000473612.1:n.172+43T>G
NM_013319.2:c.529+43T>G	NP_037451.1:n.529+43T>G
XM_006710590.2:c.529+43T>G	XP_006710653.1:n.529+43T>G
XM_011541304.1:c.529+43T>G	XP_011539606.1:n.529+43T>G
XR_946616.1:n.863+43T>G
NM_001330349.1:c.529+43T>G	NP_001317278.1:n.529+43T>G
NM_001330350.1:c.529+43T>G	NP_001317279.1:n.529+43T>G
XR_946616.3:n.863+43T>G
NM_001330349.2:c.529+43T>G	NP_001317278.1:n.529+43T>G
NM_001330350.2:c.529+43T>G	NP_001317279.1:n.529+43T>G
NM_013319.3:c.529+43T>G MANE Select	NP_037451.1:n.529+43T>G