Canonical Allele Identifier: CA414895219
Gene: DKC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154773170A>C , CM000685.2:g.154773170A>C GRCh38
NC_000023.10:g.154001445A>C , CM000685.1:g.154001445A>C GRCh37
NC_000023.9:g.153654639A>C NCBI36
NG_009780.1:g.15415A>C , LRG_55:g.15415A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.956A>C ENSP00000400542.2:p.Asp319Ala
ENST00000426673.6:c.*459A>C ENSP00000407253.3:n.*459A>C
ENST00000484317.6:n.861A>C
ENST00000696575.1:c.1076A>C ENSP00000512730.1:p.Asp359Ala
ENST00000696577.1:c.1076A>C ENSP00000512731.1:p.Asp359Ala
ENST00000696578.1:c.*28A>C ENSP00000512732.1:n.*28A>C
ENST00000696579.1:n.1178A>C
ENST00000696580.1:c.989A>C ENSP00000512733.1:p.Asp330Ala
ENST00000696581.1:c.*1050A>C ENSP00000512734.1:n.*1050A>C
ENST00000696582.1:c.*282A>C ENSP00000512735.1:n.*282A>C
ENST00000696583.1:c.1037A>C ENSP00000512736.1:p.Asp346Ala
ENST00000696584.1:n.1600A>C
ENST00000696585.1:n.1719A>C
ENST00000696586.1:n.1493A>C
ENST00000696587.1:c.956A>C ENSP00000512737.1:p.Asp319Ala
ENST00000696588.1:c.467A>C ENSP00000513251.1:p.Asp156Ala
ENST00000696589.1:n.851A>C
ENST00000696590.1:n.700A>C
ENST00000696591.1:n.425A>C
ENST00000696592.1:n.1955A>C
ENST00000696627.1:c.1076A>C ENSP00000512764.1:p.Asp359Ala
ENST00000696628.1:c.1076A>C ENSP00000512765.1:p.Asp359Ala
ENST00000369550.10:c.1076A>C MANE Select ENSP00000358563.5:p.Asp359Ala
ENST00000369550.9:c.1076A>C ENSP00000358563.5:p.Asp359Ala
ENST00000412124.5:c.334A>C
ENST00000426673.5:c.436A>C
ENST00000475966.1:n.565A>C
ENST00000481062.1:n.27A>C
ENST00000620277.4:c.1076A>C ENSP00000478387.1:p.Asp359Ala
NM_001142463.2:c.1076A>C NP_001135935.1:p.Asp359Ala
NM_001288747.1:c.1076A>C NP_001275676.1:p.Asp359Ala
NM_001363.4:c.1076A>C NP_001354.1:p.Asp359Ala
NR_110021.1:n.1777A>C
NR_110022.1:n.1896A>C
NR_110023.1:n.1670A>C
NM_001363.5:c.1076A>C MANE Select NP_001354.1:p.Asp359Ala
NM_001142463.3:c.1076A>C NP_001135935.1:p.Asp359Ala
NR_110021.2:n.1655A>C
NR_110022.2:n.1774A>C
NR_110023.2:n.1548A>C
NM_001288747.2:c.1076A>C NP_001275676.1:p.Asp359Ala