Canonical Allele Identifier: CA416045163
Gene: UBIAD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11333855G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273798G>C , CM000663.2:g.11273798G>C GRCh38
NC_000001.10:g.11333855G>C , CM000663.1:g.11333855G>C GRCh37
NC_000001.9:g.11256442G>C NCBI36
NG_009443.1:g.5601G>C
NG_009443.2:g.5601G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376810.6:c.267G>C MANE Select ENSP00000366006.5:p.Val89=
ENST00000376804.2:c.267G>C ENSP00000366000.1:p.Val89=
ENST00000376810.5:c.267G>C ENSP00000366006.5:p.Val89=
NM_013319.2:c.267G>C NP_037451.1:p.Val89=
XM_006710590.2:c.267G>C XP_006710653.1:p.Val89=
XM_011541304.1:c.267G>C XP_011539606.1:p.Val89=
XR_946616.1:n.601G>C
NM_001330349.1:c.267G>C NP_001317278.1:p.Val89=
NM_001330350.1:c.267G>C NP_001317279.1:p.Val89=
XR_946616.3:n.601G>C
NM_001330349.2:c.267G>C NP_001317278.1:p.Val89=
NM_001330350.2:c.267G>C NP_001317279.1:p.Val89=
NM_013319.3:c.267G>C MANE Select NP_037451.1:p.Val89=