Canonical Allele Identifier: CA338691440
Gene: UBIAD1 HGNC NCBI

Linked Data

gnomAD v4: 1-11273932-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273932T>C , CM000663.2:g.11273932T>C GRCh38
NC_000001.10:g.11333989T>C , CM000663.1:g.11333989T>C GRCh37
NC_000001.9:g.11256576T>C NCBI36
NG_009443.1:g.5735T>C
NG_009443.2:g.5735T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.401T>C MANE Select ENSP00000366006.5:p.Phe134Ser
ENST00000376804.2:c.401T>C ENSP00000366000.1:p.Phe134Ser
ENST00000376810.5:c.401T>C ENSP00000366006.5:p.Phe134Ser
ENST00000486588.6:c.44T>C ENSP00000473612.1:p.Phe15Ser
NM_013319.2:c.401T>C NP_037451.1:p.Phe134Ser
XM_006710590.2:c.401T>C XP_006710653.1:p.Phe134Ser
XM_011541304.1:c.401T>C XP_011539606.1:p.Phe134Ser
XR_946616.1:n.735T>C
NM_001330349.1:c.401T>C NP_001317278.1:p.Phe134Ser
NM_001330350.1:c.401T>C NP_001317279.1:p.Phe134Ser
XR_946616.3:n.735T>C
NM_001330349.2:c.401T>C NP_001317278.1:p.Phe134Ser
NM_001330350.2:c.401T>C NP_001317279.1:p.Phe134Ser
NM_013319.3:c.401T>C MANE Select NP_037451.1:p.Phe134Ser