Canonical Allele Identifier: CA18415486

Gene: UBIAD1

Linked Data

• dbSNP Id: rs965233798
• gnomAD v2: 1-11333972-G-C
• gnomAD v3: 1-11273915-G-C
• gnomAD v4: 1-11273915-G-C
• MyVariant Identifiers: chr1:g.11333972G>C (hg19) ; chr1:g.11273915G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11273915G>C , CM000663.2:g.11273915G>C	GRCh38
NC_000001.10:g.11333972G>C , CM000663.1:g.11333972G>C	GRCh37
NC_000001.9:g.11256559G>C	NCBI36
NG_009443.1:g.5718G>C
NG_009443.2:g.5718G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376810.6:c.384G>C MANE Select	ENSP00000366006.5:p.Pro128=
ENST00000376804.2:c.384G>C	ENSP00000366000.1:p.Pro128=
ENST00000376810.5:c.384G>C	ENSP00000366006.5:p.Pro128=
ENST00000486588.6:c.27G>C	ENSP00000473612.1:p.Pro9=
NM_013319.2:c.384G>C	NP_037451.1:p.Pro128=
XM_006710590.2:c.384G>C	XP_006710653.1:p.Pro128=
XM_011541304.1:c.384G>C	XP_011539606.1:p.Pro128=
XR_946616.1:n.718G>C
NM_001330349.1:c.384G>C	NP_001317278.1:p.Pro128=
NM_001330350.1:c.384G>C	NP_001317279.1:p.Pro128=
XR_946616.3:n.718G>C
NM_001330349.2:c.384G>C	NP_001317278.1:p.Pro128=
NM_001330350.2:c.384G>C	NP_001317279.1:p.Pro128=
NM_013319.3:c.384G>C MANE Select	NP_037451.1:p.Pro128=