Canonical Allele Identifier: CA2466785815
Gene: DKC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154769171A= , CM000685.2:g.154769171A= GRCh38
NC_000023.10:g.153997446A= , CM000685.1:g.153997446A= GRCh37
NC_000023.9:g.153650640A= NCBI36
NG_009780.1:g.11416A= , LRG_55:g.11416A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.656A= ENSP00000400542.2:p.His219=
ENST00000426673.6:c.*159A= ENSP00000407253.3:n.*159A=
ENST00000484317.6:n.561A=
ENST00000696575.1:c.776A= ENSP00000512730.1:p.His259=
ENST00000696576.1:n.878A=
ENST00000696577.1:c.776A= ENSP00000512731.1:p.His259=
ENST00000696578.1:c.776A= ENSP00000512732.1:p.His259=
ENST00000696579.1:n.878A=
ENST00000696580.1:c.689A= ENSP00000512733.1:p.His230=
ENST00000696581.1:c.*750A= ENSP00000512734.1:n.*750A=
ENST00000696582.1:c.645A= ENSP00000512735.1:p.Pro215=
ENST00000696583.1:c.772-35A= ENSP00000512736.1:n.772-35A=
ENST00000696584.1:n.1300A=
ENST00000696585.1:n.1419A=
ENST00000696586.1:n.1193A=
ENST00000696587.1:c.656A= ENSP00000512737.1:p.His219=
ENST00000696588.1:c.167A= ENSP00000513251.1:p.His56=
ENST00000696589.1:n.551A=
ENST00000696590.1:n.400A=
ENST00000696591.1:n.125A=
ENST00000696627.1:c.776A= ENSP00000512764.1:p.His259=
ENST00000696628.1:c.776A= ENSP00000512765.1:p.His259=
ENST00000369550.10:c.776A= MANE Select ENSP00000358563.5:p.His259=
ENST00000369550.9:c.776A= ENSP00000358563.5:p.His259=
ENST00000412124.5:c.174-1588A=
ENST00000413910.5:c.656A= ENSP00000400542.1:p.His219=
ENST00000426673.5:c.136A=
ENST00000452771.5:c.669A= ENSP00000407325.1:n.669A=
ENST00000475966.1:n.265A=
ENST00000484317.5:n.414A=
ENST00000620277.4:c.776A= ENSP00000478387.1:p.His259=
NM_001142463.2:c.776A= NP_001135935.1:p.His259=
NM_001288747.1:c.776A= NP_001275676.1:p.His259=
NM_001363.4:c.776A= NP_001354.1:p.His259=
NR_110021.1:n.1477A=
NR_110022.1:n.1596A=
NR_110023.1:n.1370A=
NM_001363.5:c.776A= MANE Select NP_001354.1:p.His259=
NM_001142463.3:c.776A= NP_001135935.1:p.His259=
NR_110021.2:n.1355A=
NR_110022.2:n.1474A=
NR_110023.2:n.1248A=
NM_001288747.2:c.776A= NP_001275676.1:p.His259=