Canonical Allele Identifier: CA416045191
Gene: UBIAD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11333894C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273837C>T , CM000663.2:g.11273837C>T GRCh38
NC_000001.10:g.11333894C>T , CM000663.1:g.11333894C>T GRCh37
NC_000001.9:g.11256481C>T NCBI36
NG_009443.1:g.5640C>T
NG_009443.2:g.5640C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.306C>T MANE Select ENSP00000366006.5:p.Asn102=
ENST00000376804.2:c.306C>T ENSP00000366000.1:p.Asn102=
ENST00000376810.5:c.306C>T ENSP00000366006.5:p.Asn102=
NM_013319.2:c.306C>T NP_037451.1:p.Asn102=
XM_006710590.2:c.306C>T XP_006710653.1:p.Asn102=
XM_011541304.1:c.306C>T XP_011539606.1:p.Asn102=
XR_946616.1:n.640C>T
NM_001330349.1:c.306C>T NP_001317278.1:p.Asn102=
NM_001330350.1:c.306C>T NP_001317279.1:p.Asn102=
XR_946616.3:n.640C>T
NM_001330349.2:c.306C>T NP_001317278.1:p.Asn102=
NM_001330350.2:c.306C>T NP_001317279.1:p.Asn102=
NM_013319.3:c.306C>T MANE Select NP_037451.1:p.Asn102=