Canonical Allele Identifier: CA414896003
Gene: DKC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154773221A>G , CM000685.2:g.154773221A>G GRCh38
NC_000023.10:g.154001496A>G , CM000685.1:g.154001496A>G GRCh37
NC_000023.9:g.153654690A>G NCBI36
NG_009780.1:g.15466A>G , LRG_55:g.15466A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.1007A>G ENSP00000400542.2:p.Tyr336Cys
ENST00000426673.6:c.*510A>G ENSP00000407253.3:n.*510A>G
ENST00000484317.6:n.912A>G
ENST00000696575.1:c.1127A>G ENSP00000512730.1:p.Tyr376Cys
ENST00000696577.1:c.1127A>G ENSP00000512731.1:p.Tyr376Cys
ENST00000696578.1:c.*79A>G ENSP00000512732.1:n.*79A>G
ENST00000696579.1:n.1229A>G
ENST00000696580.1:c.1040A>G ENSP00000512733.1:p.Tyr347Cys
ENST00000696581.1:c.*1101A>G ENSP00000512734.1:n.*1101A>G
ENST00000696582.1:c.*333A>G ENSP00000512735.1:n.*333A>G
ENST00000696583.1:c.1088A>G ENSP00000512736.1:p.Tyr363Cys
ENST00000696584.1:n.1651A>G
ENST00000696585.1:n.1770A>G
ENST00000696586.1:n.1544A>G
ENST00000696587.1:c.1007A>G ENSP00000512737.1:p.Tyr336Cys
ENST00000696588.1:c.518A>G ENSP00000513251.1:p.Tyr173Cys
ENST00000696589.1:n.902A>G
ENST00000696590.1:n.751A>G
ENST00000696591.1:n.476A>G
ENST00000696592.1:n.2006A>G
ENST00000696627.1:c.1127A>G ENSP00000512764.1:p.Tyr376Cys
ENST00000696628.1:c.1127A>G ENSP00000512765.1:p.Tyr376Cys
ENST00000369550.10:c.1127A>G MANE Select ENSP00000358563.5:p.Tyr376Cys
ENST00000369550.9:c.1127A>G ENSP00000358563.5:p.Tyr376Cys
ENST00000412124.5:c.385A>G
ENST00000426673.5:c.487A>G
ENST00000475966.1:n.616A>G
ENST00000481062.1:n.78A>G
ENST00000620277.4:c.1127A>G ENSP00000478387.1:p.Tyr376Cys
NM_001142463.2:c.1127A>G NP_001135935.1:p.Tyr376Cys
NM_001288747.1:c.1127A>G NP_001275676.1:p.Tyr376Cys
NM_001363.4:c.1127A>G NP_001354.1:p.Tyr376Cys
NR_110021.1:n.1828A>G
NR_110022.1:n.1947A>G
NR_110023.1:n.1721A>G
NM_001363.5:c.1127A>G MANE Select NP_001354.1:p.Tyr376Cys
NM_001142463.3:c.1127A>G NP_001135935.1:p.Tyr376Cys
NR_110021.2:n.1706A>G
NR_110022.2:n.1825A>G
NR_110023.2:n.1599A>G
NM_001288747.2:c.1127A>G NP_001275676.1:p.Tyr376Cys