Canonical Allele Identifier: CA416045247
Gene: UBIAD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11333943A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273886A>C , CM000663.2:g.11273886A>C GRCh38
NC_000001.10:g.11333943A>C , CM000663.1:g.11333943A>C GRCh37
NC_000001.9:g.11256530A>C NCBI36
NG_009443.1:g.5689A>C
NG_009443.2:g.5689A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376810.6:c.355A>C MANE Select ENSP00000366006.5:p.Arg119=
ENST00000376804.2:c.355A>C ENSP00000366000.1:p.Arg119=
ENST00000376810.5:c.355A>C ENSP00000366006.5:p.Arg119=
NM_013319.2:c.355A>C NP_037451.1:p.Arg119=
XM_006710590.2:c.355A>C XP_006710653.1:p.Arg119=
XM_011541304.1:c.355A>C XP_011539606.1:p.Arg119=
XR_946616.1:n.689A>C
NM_001330349.1:c.355A>C NP_001317278.1:p.Arg119=
NM_001330350.1:c.355A>C NP_001317279.1:p.Arg119=
XR_946616.3:n.689A>C
NM_001330349.2:c.355A>C NP_001317278.1:p.Arg119=
NM_001330350.2:c.355A>C NP_001317279.1:p.Arg119=
NM_013319.3:c.355A>C MANE Select NP_037451.1:p.Arg119=