Canonical Allele Identifier: CA998592094
Gene: UBIAD1 HGNC NCBI

Linked Data

dbSNP Id: rs1651883385

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273822dup , CM000663.2:g.11273822dup GRCh38
NC_000001.10:g.11333879dup , CM000663.1:g.11333879dup GRCh37
NC_000001.9:g.11256466dup NCBI36
NG_009443.1:g.5625dup
NG_009443.2:g.5625dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.291dup MANE Select ENSP00000366006.5:p.Gly98ArgfsTer2
ENST00000376804.2:c.291dup ENSP00000366000.1:p.Gly98ArgfsTer2
ENST00000376810.5:c.291dup ENSP00000366006.5:p.Gly98ArgfsTer2
NM_013319.2:c.291dup NP_037451.1:p.Gly98ArgfsTer2
XM_006710590.2:c.291dup XP_006710653.1:p.Gly98ArgfsTer2
XM_011541304.1:c.291dup XP_011539606.1:p.Gly98ArgfsTer2
XR_946616.1:n.625dup
NM_001330349.1:c.291dup NP_001317278.1:p.Gly98ArgfsTer2
NM_001330350.1:c.291dup NP_001317279.1:p.Gly98ArgfsTer2
XR_946616.3:n.625dup
NM_001330349.2:c.291dup NP_001317278.1:p.Gly98ArgfsTer2
NM_001330350.2:c.291dup NP_001317279.1:p.Gly98ArgfsTer2
NM_013319.3:c.291dup MANE Select NP_037451.1:p.Gly98ArgfsTer2