Canonical Allele Identifier: CA4329975
Gene: DBF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87908129C>T , CM000669.2:g.87908129C>T GRCh38
NC_000007.13:g.87537444C>T , CM000669.1:g.87537444C>T GRCh37
NC_000007.12:g.87375380C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006716.4:c.1991C>T MANE Select NP_006707.1:p.Ser664Leu
ENST00000265728.6:c.1991C>T MANE Select ENSP00000265728.1:p.Ser664Leu
NM_001318060.1:c.1292C>T NP_001304989.1:p.Ser431Leu
NM_001318060.2:c.1292C>T NP_001304989.1:p.Ser431Leu
NM_001318061.1:c.1319C>T NP_001304990.1:p.Ser440Leu
NM_001318061.2:c.1319C>T NP_001304990.1:p.Ser440Leu
NM_001318062.1:c.1211C>T NP_001304991.1:p.Ser404Leu
NM_001318062.2:c.1211C>T NP_001304991.1:p.Ser404Leu
NM_006716.3:c.1991C>T NP_006707.1:p.Ser664Leu
ENST00000265728.5:c.1991C>T ENSP00000265728.1:p.Ser664Leu
ENST00000413643.5:c.*1225C>T ENSP00000414083.1:n.*1225C>T
ENST00000431138.5:c.*1764C>T ENSP00000407116.1:n.*1764C>T
XM_005250120.2:c.1988C>T XP_005250177.1:p.Ser663Leu
XM_005250121.2:c.1319C>T XP_005250178.1:p.Ser440Leu
XM_006715843.2:c.1319C>T XP_006715906.1:p.Ser440Leu
XM_011515764.1:c.1940C>T XP_011514066.1:p.Ser647Leu
XM_011515765.1:c.1211C>T XP_011514067.1:p.Ser404Leu
XR_927343.1:n.2208C>T
XR_927723.1:n.148+5772G>A
XR_927724.1:n.192+5772G>A