Canonical Allele Identifier: CA2466788302
Gene: DKC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154776231A= , CM000685.2:g.154776231A= GRCh38
NC_000023.10:g.154004506A= , CM000685.1:g.154004506A= GRCh37
NC_000023.9:g.153657700A= NCBI36
NG_009780.1:g.18476A= , LRG_55:g.18476A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.*179A= ENSP00000400542.2:n.*179A=
ENST00000426673.6:c.*825A= ENSP00000407253.3:n.*825A=
ENST00000484317.6:n.1657A=
ENST00000492372.2:n.321A=
ENST00000696575.1:c.1368A= ENSP00000512730.1:p.Ala456=
ENST00000696577.1:c.1383A= ENSP00000512731.1:p.Ala461=
ENST00000696578.1:c.*335A= ENSP00000512732.1:n.*335A=
ENST00000696579.1:n.2398A=
ENST00000696580.1:c.1296A= ENSP00000512733.1:p.Ala432=
ENST00000696581.1:c.*1357A= ENSP00000512734.1:n.*1357A=
ENST00000696582.1:c.*589A= ENSP00000512735.1:n.*589A=
ENST00000696583.1:c.1344A= ENSP00000512736.1:p.Ala448=
ENST00000696584.1:n.1907A=
ENST00000696585.1:n.2026A=
ENST00000696586.1:n.1800A=
ENST00000696587.1:c.1263A= ENSP00000512737.1:p.Ala421=
ENST00000696588.1:c.774A= ENSP00000513251.1:p.Ala258=
ENST00000696589.1:n.1158A=
ENST00000696590.1:n.2409A=
ENST00000696591.1:n.732A=
ENST00000696592.1:n.3664A=
ENST00000696627.1:c.*209A= ENSP00000512764.1:n.*209A=
ENST00000696628.1:c.1383A= ENSP00000512765.1:p.Ala461=
ENST00000369550.10:c.1383A= MANE Select ENSP00000358563.5:p.Ala461=
ENST00000369550.9:c.1383A= ENSP00000358563.5:p.Ala461=
ENST00000412124.5:c.641A=
ENST00000426673.5:c.802A=
ENST00000475966.1:n.872A=
ENST00000492372.1:n.200A=
ENST00000620277.4:c.*609A= ENSP00000478387.1:n.*609A=
NM_001142463.2:c.1368A= NP_001135935.1:p.Ala456=
NM_001288747.1:c.*609A= NP_001275676.1:n.*609A=
NM_001363.4:c.1383A= NP_001354.1:p.Ala461=
NR_110021.1:n.2084A=
NR_110022.1:n.2203A=
NR_110023.1:n.1977A=
NM_001363.5:c.1383A= MANE Select NP_001354.1:p.Ala461=
NM_001142463.3:c.1368A= NP_001135935.1:p.Ala456=
NR_110021.2:n.1962A=
NR_110022.2:n.2081A=
NR_110023.2:n.1855A=
NM_001288747.2:c.*609A= NP_001275676.1:n.*609A=