Canonical Allele Identifier: CA2466785817
Gene: DKC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154769175G= , CM000685.2:g.154769175G= GRCh38
NC_000023.10:g.153997450G= , CM000685.1:g.153997450G= GRCh37
NC_000023.9:g.153650644G= NCBI36
NG_009780.1:g.11420G= , LRG_55:g.11420G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.660G= ENSP00000400542.2:p.Met220=
ENST00000426673.6:c.*163G= ENSP00000407253.3:n.*163G=
ENST00000484317.6:n.565G=
ENST00000696575.1:c.780G= ENSP00000512730.1:p.Met260=
ENST00000696576.1:n.882G=
ENST00000696577.1:c.780G= ENSP00000512731.1:p.Met260=
ENST00000696578.1:c.780G= ENSP00000512732.1:p.Met260=
ENST00000696579.1:n.882G=
ENST00000696580.1:c.693G= ENSP00000512733.1:p.Met231=
ENST00000696581.1:c.*754G= ENSP00000512734.1:n.*754G=
ENST00000696582.1:c.649G= ENSP00000512735.1:p.Gly217=
ENST00000696583.1:c.772-31G= ENSP00000512736.1:n.772-31G=
ENST00000696584.1:n.1304G=
ENST00000696585.1:n.1423G=
ENST00000696586.1:n.1197G=
ENST00000696587.1:c.660G= ENSP00000512737.1:p.Met220=
ENST00000696588.1:c.171G= ENSP00000513251.1:p.Met57=
ENST00000696589.1:n.555G=
ENST00000696590.1:n.404G=
ENST00000696591.1:n.129G=
ENST00000696627.1:c.780G= ENSP00000512764.1:p.Met260=
ENST00000696628.1:c.780G= ENSP00000512765.1:p.Met260=
ENST00000369550.10:c.780G= MANE Select ENSP00000358563.5:p.Met260=
ENST00000369550.9:c.780G= ENSP00000358563.5:p.Met260=
ENST00000412124.5:c.174-1584G=
ENST00000413910.5:c.660G= ENSP00000400542.1:p.Met220=
ENST00000426673.5:c.140G=
ENST00000452771.5:c.673G= ENSP00000407325.1:n.673G=
ENST00000475966.1:n.269G=
ENST00000484317.5:n.418G=
ENST00000620277.4:c.780G= ENSP00000478387.1:p.Met260=
NM_001142463.2:c.780G= NP_001135935.1:p.Met260=
NM_001288747.1:c.780G= NP_001275676.1:p.Met260=
NM_001363.4:c.780G= NP_001354.1:p.Met260=
NR_110021.1:n.1481G=
NR_110022.1:n.1600G=
NR_110023.1:n.1374G=
NM_001363.5:c.780G= MANE Select NP_001354.1:p.Met260=
NM_001142463.3:c.780G= NP_001135935.1:p.Met260=
NR_110021.2:n.1359G=
NR_110022.2:n.1478G=
NR_110023.2:n.1252G=
NM_001288747.2:c.780G= NP_001275676.1:p.Met260=