Canonical Allele Identifier: CA414896042
Gene: DKC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154773226C>G , CM000685.2:g.154773226C>G GRCh38
NC_000023.10:g.154001501C>G , CM000685.1:g.154001501C>G GRCh37
NC_000023.9:g.153654695C>G NCBI36
NG_009780.1:g.15471C>G , LRG_55:g.15471C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.1012C>G ENSP00000400542.2:p.Arg338Gly
ENST00000426673.6:c.*515C>G ENSP00000407253.3:n.*515C>G
ENST00000484317.6:n.917C>G
ENST00000696575.1:c.1132C>G ENSP00000512730.1:p.Arg378Gly
ENST00000696577.1:c.1132C>G ENSP00000512731.1:p.Arg378Gly
ENST00000696578.1:c.*84C>G ENSP00000512732.1:n.*84C>G
ENST00000696579.1:n.1234C>G
ENST00000696580.1:c.1045C>G ENSP00000512733.1:p.Arg349Gly
ENST00000696581.1:c.*1106C>G ENSP00000512734.1:n.*1106C>G
ENST00000696582.1:c.*338C>G ENSP00000512735.1:n.*338C>G
ENST00000696583.1:c.1093C>G ENSP00000512736.1:p.Arg365Gly
ENST00000696584.1:n.1656C>G
ENST00000696585.1:n.1775C>G
ENST00000696586.1:n.1549C>G
ENST00000696587.1:c.1012C>G ENSP00000512737.1:p.Arg338Gly
ENST00000696588.1:c.523C>G ENSP00000513251.1:p.Arg175Gly
ENST00000696589.1:n.907C>G
ENST00000696590.1:n.756C>G
ENST00000696591.1:n.481C>G
ENST00000696592.1:n.2011C>G
ENST00000696627.1:c.1132C>G ENSP00000512764.1:p.Arg378Gly
ENST00000696628.1:c.1132C>G ENSP00000512765.1:p.Arg378Gly
ENST00000369550.10:c.1132C>G MANE Select ENSP00000358563.5:p.Arg378Gly
ENST00000369550.9:c.1132C>G ENSP00000358563.5:p.Arg378Gly
ENST00000412124.5:c.390C>G
ENST00000426673.5:c.492C>G
ENST00000475966.1:n.621C>G
ENST00000481062.1:n.83C>G
ENST00000620277.4:c.1132C>G ENSP00000478387.1:p.Arg378Gly
NM_001142463.2:c.1132C>G NP_001135935.1:p.Arg378Gly
NM_001288747.1:c.1132C>G NP_001275676.1:p.Arg378Gly
NM_001363.4:c.1132C>G NP_001354.1:p.Arg378Gly
NR_110021.1:n.1833C>G
NR_110022.1:n.1952C>G
NR_110023.1:n.1726C>G
NM_001363.5:c.1132C>G MANE Select NP_001354.1:p.Arg378Gly
NM_001142463.3:c.1132C>G NP_001135935.1:p.Arg378Gly
NR_110021.2:n.1711C>G
NR_110022.2:n.1830C>G
NR_110023.2:n.1604C>G
NM_001288747.2:c.1132C>G NP_001275676.1:p.Arg378Gly