Canonical Allele Identifier: CA416045379
Gene: UBIAD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11334059G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11274002G>C , CM000663.2:g.11274002G>C GRCh38
NC_000001.10:g.11334059G>C , CM000663.1:g.11334059G>C GRCh37
NC_000001.9:g.11256646G>C NCBI36
NG_009443.1:g.5805G>C
NG_009443.2:g.5805G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.471G>C MANE Select ENSP00000366006.5:p.Leu157=
ENST00000376804.2:c.471G>C ENSP00000366000.1:p.Leu157=
ENST00000376810.5:c.471G>C ENSP00000366006.5:p.Leu157=
ENST00000483738.1:c.69G>C ENSP00000473453.1:p.Leu23=
ENST00000486588.6:c.114G>C ENSP00000473612.1:p.Leu38=
NM_013319.2:c.471G>C NP_037451.1:p.Leu157=
XM_006710590.2:c.471G>C XP_006710653.1:p.Leu157=
XM_011541304.1:c.471G>C XP_011539606.1:p.Leu157=
XR_946616.1:n.805G>C
NM_001330349.1:c.471G>C NP_001317278.1:p.Leu157=
NM_001330350.1:c.471G>C NP_001317279.1:p.Leu157=
XR_946616.3:n.805G>C
NM_001330349.2:c.471G>C NP_001317278.1:p.Leu157=
NM_001330350.2:c.471G>C NP_001317279.1:p.Leu157=
NM_013319.3:c.471G>C MANE Select NP_037451.1:p.Leu157=