Canonical Allele Identifier: CA2830536685
Gene: DCUN1D4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.51886732G>T , CM000666.2:g.51886732G>T GRCh38
NC_000004.11:g.52752898G>T , CM000666.1:g.52752898G>T GRCh37
NC_000004.10:g.52447655G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334635.10:c.414+94G>T MANE Select ENSP00000334625.5:n.414+94G>T
ENST00000334635.9:c.414+94G>T ENSP00000334625.5:n.414+94G>T
ENST00000381441.7:c.414+94G>T ENSP00000370850.3:n.414+94G>T
ENST00000451288.6:c.546+94G>T ENSP00000389900.2:n.546+94G>T
ENST00000477560.5:c.*76G>T ENSP00000424476.1:n.*76G>T
ENST00000502930.5:c.*233+94G>T ENSP00000425792.1:n.*233+94G>T
ENST00000504113.5:n.526+94G>T
ENST00000504923.5:n.470+94G>T
ENST00000505403.5:c.546+94G>T ENSP00000426982.1:n.546+94G>T
ENST00000505634.5:c.71+94G>T
ENST00000507659.5:n.120+94G>T
ENST00000507741.5:c.*502+94G>T ENSP00000423808.1:n.*502+94G>T
ENST00000509068.5:c.546+94G>T ENSP00000421699.1:n.546+94G>T
ENST00000509376.5:c.*327G>T ENSP00000425644.1:n.*327G>T
ENST00000510587.5:n.229+94G>T
NM_001040402.2:c.414+94G>T NP_001035492.1:n.414+94G>T
NM_001287755.1:c.546+94G>T NP_001274684.1:n.546+94G>T
NM_001287757.1:c.234+94G>T NP_001274686.1:n.234+94G>T
NM_015115.3:c.414+94G>T NP_055930.2:n.414+94G>T
XM_005265731.2:c.546+94G>T XP_005265788.1:n.546+94G>T
XM_011534379.1:c.420+94G>T XP_011532681.1:n.420+94G>T
XM_011534380.1:c.234+94G>T XP_011532682.1:n.234+94G>T
XR_245254.2:n.561+94G>T
XR_427521.2:n.561+94G>T
XR_941045.1:n.561+94G>T
XR_941046.1:n.561+94G>T
XM_005265731.3:c.546+94G>T XP_005265788.1:n.546+94G>T
XM_011534379.2:c.420+94G>T XP_011532681.1:n.420+94G>T
XM_017007912.2:c.420+94G>T XP_016863401.1:n.420+94G>T
XM_017007913.2:c.-519G>T XP_016863402.1:n.-519G>T
XM_024453941.1:c.234+94G>T XP_024309709.1:n.234+94G>T
XM_024453942.1:c.234+94G>T XP_024309710.1:n.234+94G>T
XM_024453943.1:c.234+94G>T XP_024309711.1:n.234+94G>T
XM_024453944.1:c.234+94G>T XP_024309712.1:n.234+94G>T
XM_024453945.1:c.234+94G>T XP_024309713.1:n.234+94G>T
XR_001741175.1:n.547+94G>T
XR_001741176.1:n.547+94G>T
XR_001741177.2:n.525+94G>T
XR_001741178.2:n.525+94G>T
XR_001741179.2:n.525+94G>T
XR_001741180.2:n.525+94G>T
XR_245254.3:n.547+94G>T
XR_427521.3:n.547+94G>T
XR_941046.2:n.547+94G>T
NM_001040402.3:c.414+94G>T MANE Select NP_001035492.1:n.414+94G>T
NM_001287757.2:c.234+94G>T NP_001274686.1:n.234+94G>T
NM_015115.4:c.414+94G>T NP_055930.2:n.414+94G>T