Canonical Allele Identifier: CA414896080
Gene: DKC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154773232T>A , CM000685.2:g.154773232T>A GRCh38
NC_000023.10:g.154001507T>A , CM000685.1:g.154001507T>A GRCh37
NC_000023.9:g.153654701T>A NCBI36
NG_009780.1:g.15477T>A , LRG_55:g.15477T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.1018T>A ENSP00000400542.2:p.Trp340Arg
ENST00000426673.6:c.*521T>A ENSP00000407253.3:n.*521T>A
ENST00000484317.6:n.923T>A
ENST00000696575.1:c.1138T>A ENSP00000512730.1:p.Trp380Arg
ENST00000696577.1:c.1138T>A ENSP00000512731.1:p.Trp380Arg
ENST00000696578.1:c.*90T>A ENSP00000512732.1:n.*90T>A
ENST00000696579.1:n.1240T>A
ENST00000696580.1:c.1051T>A ENSP00000512733.1:p.Trp351Arg
ENST00000696581.1:c.*1112T>A ENSP00000512734.1:n.*1112T>A
ENST00000696582.1:c.*344T>A ENSP00000512735.1:n.*344T>A
ENST00000696583.1:c.1099T>A ENSP00000512736.1:p.Trp367Arg
ENST00000696584.1:n.1662T>A
ENST00000696585.1:n.1781T>A
ENST00000696586.1:n.1555T>A
ENST00000696587.1:c.1018T>A ENSP00000512737.1:p.Trp340Arg
ENST00000696588.1:c.529T>A ENSP00000513251.1:p.Trp177Arg
ENST00000696589.1:n.913T>A
ENST00000696590.1:n.762T>A
ENST00000696591.1:n.487T>A
ENST00000696592.1:n.2017T>A
ENST00000696627.1:c.1138T>A ENSP00000512764.1:p.Trp380Arg
ENST00000696628.1:c.1138T>A ENSP00000512765.1:p.Trp380Arg
ENST00000369550.10:c.1138T>A MANE Select ENSP00000358563.5:p.Trp380Arg
ENST00000369550.9:c.1138T>A ENSP00000358563.5:p.Trp380Arg
ENST00000412124.5:c.396T>A
ENST00000426673.5:c.498T>A
ENST00000475966.1:n.627T>A
ENST00000481062.1:n.89T>A
ENST00000620277.4:c.1138T>A ENSP00000478387.1:p.Trp380Arg
NM_001142463.2:c.1138T>A NP_001135935.1:p.Trp380Arg
NM_001288747.1:c.1138T>A NP_001275676.1:p.Trp380Arg
NM_001363.4:c.1138T>A NP_001354.1:p.Trp380Arg
NR_110021.1:n.1839T>A
NR_110022.1:n.1958T>A
NR_110023.1:n.1732T>A
NM_001363.5:c.1138T>A MANE Select NP_001354.1:p.Trp380Arg
NM_001142463.3:c.1138T>A NP_001135935.1:p.Trp380Arg
NR_110021.2:n.1717T>A
NR_110022.2:n.1836T>A
NR_110023.2:n.1610T>A
NM_001288747.2:c.1138T>A NP_001275676.1:p.Trp380Arg