Canonical Allele Identifier: CA2643253670
Gene: UBIAD1 HGNC NCBI

Linked Data

gnomAD v4: 1-11274139-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11274139G>T , CM000663.2:g.11274139G>T GRCh38
NC_000001.10:g.11334196G>T , CM000663.1:g.11334196G>T GRCh37
NC_000001.9:g.11256783G>T NCBI36
NG_009443.1:g.5942G>T
NG_009443.2:g.5942G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.529+79G>T MANE Select ENSP00000366006.5:n.529+79G>T
ENST00000376804.2:c.529+79G>T ENSP00000366000.1:n.529+79G>T
ENST00000376810.5:c.529+79G>T ENSP00000366006.5:n.529+79G>T
ENST00000483738.1:c.127+79G>T ENSP00000473453.1:n.127+79G>T
ENST00000486588.6:c.172+79G>T ENSP00000473612.1:n.172+79G>T
NM_013319.2:c.529+79G>T NP_037451.1:n.529+79G>T
XM_006710590.2:c.529+79G>T XP_006710653.1:n.529+79G>T
XM_011541304.1:c.529+79G>T XP_011539606.1:n.529+79G>T
XR_946616.1:n.863+79G>T
NM_001330349.1:c.529+79G>T NP_001317278.1:n.529+79G>T
NM_001330350.1:c.529+79G>T NP_001317279.1:n.529+79G>T
XR_946616.3:n.863+79G>T
NM_001330349.2:c.529+79G>T NP_001317278.1:n.529+79G>T
NM_001330350.2:c.529+79G>T NP_001317279.1:n.529+79G>T
NM_013319.3:c.529+79G>T MANE Select NP_037451.1:n.529+79G>T