Canonical Allele Identifier: CA338691502

Gene: UBIAD1

Linked Data

• dbSNP Id: rs762840240
• gnomAD v2: 1-11334018-G-T
• gnomAD v4: 1-11273961-G-T
• MyVariant Identifiers: chr1:g.11334018G>T (hg19) ; chr1:g.11273961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11273961G>T , CM000663.2:g.11273961G>T	GRCh38
NC_000001.10:g.11334018G>T , CM000663.1:g.11334018G>T	GRCh37
NC_000001.9:g.11256605G>T	NCBI36
NG_009443.1:g.5764G>T
NG_009443.2:g.5764G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376810.6:c.430G>T MANE Select	ENSP00000366006.5:p.Val144Phe
ENST00000376804.2:c.430G>T	ENSP00000366000.1:p.Val144Phe
ENST00000376810.5:c.430G>T	ENSP00000366006.5:p.Val144Phe
ENST00000483738.1:c.28G>T	ENSP00000473453.1:p.Val10Phe
ENST00000486588.6:c.73G>T	ENSP00000473612.1:p.Val25Phe
NM_013319.2:c.430G>T	NP_037451.1:p.Val144Phe
XM_006710590.2:c.430G>T	XP_006710653.1:p.Val144Phe
XM_011541304.1:c.430G>T	XP_011539606.1:p.Val144Phe
XR_946616.1:n.764G>T
NM_001330349.1:c.430G>T	NP_001317278.1:p.Val144Phe
NM_001330350.1:c.430G>T	NP_001317279.1:p.Val144Phe
XR_946616.3:n.764G>T
NM_001330349.2:c.430G>T	NP_001317278.1:p.Val144Phe
NM_001330350.2:c.430G>T	NP_001317279.1:p.Val144Phe
NM_013319.3:c.430G>T MANE Select	NP_037451.1:p.Val144Phe