Canonical Allele Identifier: CA1153587894
Gene: UBIAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11274154C= , CM000663.2:g.11274154C= GRCh38
NC_000001.10:g.11334211C= , CM000663.1:g.11334211C= GRCh37
NC_000001.9:g.11256798C= NCBI36
NG_009443.1:g.5957C=
NG_009443.2:g.5957C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.529+94C= MANE Select ENSP00000366006.5:n.529+94C=
ENST00000376804.2:c.529+94C= ENSP00000366000.1:n.529+94C=
ENST00000376810.5:c.529+94C= ENSP00000366006.5:n.529+94C=
ENST00000483738.1:c.127+94C= ENSP00000473453.1:n.127+94C=
ENST00000486588.6:c.172+94C= ENSP00000473612.1:n.172+94C=
NM_013319.2:c.529+94C= NP_037451.1:n.529+94C=
XM_006710590.2:c.529+94C= XP_006710653.1:n.529+94C=
XM_011541304.1:c.529+94C= XP_011539606.1:n.529+94C=
XR_946616.1:n.863+94C=
NM_001330349.1:c.529+94C= NP_001317278.1:n.529+94C=
NM_001330350.1:c.529+94C= NP_001317279.1:n.529+94C=
XR_946616.3:n.863+94C=
NM_001330349.2:c.529+94C= NP_001317278.1:n.529+94C=
NM_001330350.2:c.529+94C= NP_001317279.1:n.529+94C=
NM_013319.3:c.529+94C= MANE Select NP_037451.1:n.529+94C=