Canonical Allele Identifier: CA414899349
Gene: DKC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154776199A>G , CM000685.2:g.154776199A>G GRCh38
NC_000023.10:g.154004474A>G , CM000685.1:g.154004474A>G GRCh37
NC_000023.9:g.153657668A>G NCBI36
NG_009780.1:g.18444A>G , LRG_55:g.18444A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.*147A>G ENSP00000400542.2:n.*147A>G
ENST00000426673.6:c.*793A>G ENSP00000407253.3:n.*793A>G
ENST00000484317.6:n.1625A>G
ENST00000492372.2:n.289A>G
ENST00000696575.1:c.1336A>G ENSP00000512730.1:p.Ser446Gly
ENST00000696577.1:c.1351A>G ENSP00000512731.1:p.Ser451Gly
ENST00000696578.1:c.*303A>G ENSP00000512732.1:n.*303A>G
ENST00000696579.1:n.2366A>G
ENST00000696580.1:c.1264A>G ENSP00000512733.1:p.Ser422Gly
ENST00000696581.1:c.*1325A>G ENSP00000512734.1:n.*1325A>G
ENST00000696582.1:c.*557A>G ENSP00000512735.1:n.*557A>G
ENST00000696583.1:c.1312A>G ENSP00000512736.1:p.Ser438Gly
ENST00000696584.1:n.1875A>G
ENST00000696585.1:n.1994A>G
ENST00000696586.1:n.1768A>G
ENST00000696587.1:c.1231A>G ENSP00000512737.1:p.Ser411Gly
ENST00000696588.1:c.742A>G ENSP00000513251.1:p.Ser248Gly
ENST00000696589.1:n.1126A>G
ENST00000696590.1:n.2377A>G
ENST00000696591.1:n.700A>G
ENST00000696592.1:n.3632A>G
ENST00000696627.1:c.*177A>G ENSP00000512764.1:n.*177A>G
ENST00000696628.1:c.1351A>G ENSP00000512765.1:p.Ser451Gly
ENST00000369550.10:c.1351A>G MANE Select ENSP00000358563.5:p.Ser451Gly
ENST00000369550.9:c.1351A>G ENSP00000358563.5:p.Ser451Gly
ENST00000412124.5:c.609A>G
ENST00000426673.5:c.770A>G
ENST00000475966.1:n.840A>G
ENST00000492372.1:n.168A>G
ENST00000620277.4:c.*577A>G ENSP00000478387.1:n.*577A>G
NM_001142463.2:c.1336A>G NP_001135935.1:p.Ser446Gly
NM_001288747.1:c.*577A>G NP_001275676.1:n.*577A>G
NM_001363.4:c.1351A>G NP_001354.1:p.Ser451Gly
NR_110021.1:n.2052A>G
NR_110022.1:n.2171A>G
NR_110023.1:n.1945A>G
NM_001363.5:c.1351A>G MANE Select NP_001354.1:p.Ser451Gly
NM_001142463.3:c.1336A>G NP_001135935.1:p.Ser446Gly
NR_110021.2:n.1930A>G
NR_110022.2:n.2049A>G
NR_110023.2:n.1823A>G
NM_001288747.2:c.*577A>G NP_001275676.1:n.*577A>G