Canonical Allele Identifier: CA397602189
Gene: DPH1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2033523G>A , CM000679.2:g.2033523G>A GRCh38
NC_000017.10:g.1936817G>A , CM000679.1:g.1936817G>A GRCh37
NC_000017.9:g.1883567G>A NCBI36
NG_051946.1:g.8412G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263083.12:c.80G>A MANE Select ENSP00000263083.7:p.Arg27His
ENST00000570477.6:c.-146G>A ENSP00000458726.1:n.-146G>A
ENST00000571418.7:c.80G>A ENSP00000458838.2:p.Arg27His
ENST00000575667.6:c.91G>A
ENST00000674200.2:c.95G>A ENSP00000501368.1:p.Arg32His
ENST00000263083.10:c.95G>A ENSP00000263083.6:p.Arg32His
ENST00000570477.5:c.-146G>A ENSP00000458726.1:n.-146G>A
ENST00000571418.5:c.91G>A
ENST00000572819.6:n.83G>A
ENST00000575667.5:c.91G>A
ENST00000576129.5:n.64G>A
NM_001383.3:c.95G>A NP_001374.3:p.Arg32His
NM_001346574.1:c.95G>A NP_001333503.1:p.Arg32His
NM_001346575.1:c.95G>A NP_001333504.1:p.Arg32His
NM_001346576.1:c.-204G>A NP_001333505.1:n.-204G>A
NM_001383.4:c.95G>A NP_001374.3:p.Arg32His
NR_144474.1:n.138G>A
NR_144475.1:n.138G>A
NR_144476.1:n.138G>A
NM_001383.5:c.80G>A NP_001374.4:p.Arg27His
NM_001346576.2:c.-204G>A NP_001333505.1:n.-204G>A
NM_001383.6:c.80G>A MANE Select NP_001374.4:p.Arg27His
NR_144474.2:n.97G>A
NR_144475.2:n.97G>A
NR_144476.2:n.97G>A