Canonical Allele Identifier: CA591119

Gene: UBIAD1

Linked Data

• dbSNP Id: rs760910518
• ExAC: 1:11333852 C / T
• gnomAD v2: 1-11333852-C-T
• gnomAD v4: 1-11273795-C-T
• MyVariant Identifiers: chr1:g.11333852C>T (hg19) ; chr1:g.11273795C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11273795C>T , CM000663.2:g.11273795C>T	GRCh38
NC_000001.10:g.11333852C>T , CM000663.1:g.11333852C>T	GRCh37
NC_000001.9:g.11256439C>T	NCBI36
NG_009443.1:g.5598C>T
NG_009443.2:g.5598C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.264C>T MANE Select	ENSP00000366006.5:p.Ala88=
ENST00000376804.2:c.264C>T	ENSP00000366000.1:p.Ala88=
ENST00000376810.5:c.264C>T	ENSP00000366006.5:p.Ala88=
NM_013319.2:c.264C>T	NP_037451.1:p.Ala88=
XM_006710590.2:c.264C>T	XP_006710653.1:p.Ala88=
XM_011541304.1:c.264C>T	XP_011539606.1:p.Ala88=
XR_946616.1:n.598C>T
NM_001330349.1:c.264C>T	NP_001317278.1:p.Ala88=
NM_001330350.1:c.264C>T	NP_001317279.1:p.Ala88=
XR_946616.3:n.598C>T
NM_001330349.2:c.264C>T	NP_001317278.1:p.Ala88=
NM_001330350.2:c.264C>T	NP_001317279.1:p.Ala88=
NM_013319.3:c.264C>T MANE Select	NP_037451.1:p.Ala88=