Canonical Allele Identifier: CA2466787191
Gene: DKC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154773257G= , CM000685.2:g.154773257G= GRCh38
NC_000023.10:g.154001532G= , CM000685.1:g.154001532G= GRCh37
NC_000023.9:g.153654726G= NCBI36
NG_009780.1:g.15502G= , LRG_55:g.15502G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.1035+8G= ENSP00000400542.2:n.1035+8G=
ENST00000426673.6:c.*538+8G= ENSP00000407253.3:n.*538+8G=
ENST00000484317.6:n.940+8G=
ENST00000696575.1:c.1155+8G= ENSP00000512730.1:n.1155+8G=
ENST00000696577.1:c.1155+8G= ENSP00000512731.1:n.1155+8G=
ENST00000696578.1:c.*107+8G= ENSP00000512732.1:n.*107+8G=
ENST00000696579.1:n.1257+8G=
ENST00000696580.1:c.1068+8G= ENSP00000512733.1:n.1068+8G=
ENST00000696581.1:c.*1129+8G= ENSP00000512734.1:n.*1129+8G=
ENST00000696582.1:c.*361+8G= ENSP00000512735.1:n.*361+8G=
ENST00000696583.1:c.1116+8G= ENSP00000512736.1:n.1116+8G=
ENST00000696584.1:n.1679+8G=
ENST00000696585.1:n.1798+8G=
ENST00000696586.1:n.1572+8G=
ENST00000696587.1:c.1035+8G= ENSP00000512737.1:n.1035+8G=
ENST00000696588.1:c.546+8G= ENSP00000513251.1:n.546+8G=
ENST00000696589.1:n.930+8G=
ENST00000696590.1:n.779+8G=
ENST00000696591.1:n.504+8G=
ENST00000696592.1:n.2034+8G=
ENST00000696627.1:c.1159+4G= ENSP00000512764.1:n.1159+4G=
ENST00000696628.1:c.1155+8G= ENSP00000512765.1:n.1155+8G=
ENST00000369550.10:c.1155+8G= MANE Select ENSP00000358563.5:n.1155+8G=
ENST00000369550.9:c.1155+8G= ENSP00000358563.5:n.1155+8G=
ENST00000412124.5:c.413+8G=
ENST00000426673.5:c.515+8G=
ENST00000475966.1:n.644+8G=
ENST00000481062.1:n.106+8G=
ENST00000620277.4:c.1155+8G= ENSP00000478387.1:n.1155+8G=
NM_001142463.2:c.1155+8G= NP_001135935.1:n.1155+8G=
NM_001288747.1:c.1155+8G= NP_001275676.1:n.1155+8G=
NM_001363.4:c.1155+8G= NP_001354.1:n.1155+8G=
NR_110021.1:n.1856+8G=
NR_110022.1:n.1975+8G=
NR_110023.1:n.1749+8G=
NM_001363.5:c.1155+8G= MANE Select NP_001354.1:n.1155+8G=
NM_001142463.3:c.1155+8G= NP_001135935.1:n.1155+8G=
NR_110021.2:n.1734+8G=
NR_110022.2:n.1853+8G=
NR_110023.2:n.1627+8G=
NM_001288747.2:c.1155+8G= NP_001275676.1:n.1155+8G=