Canonical Allele Identifier: CA2466788300
Gene: DKC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154776224C= , CM000685.2:g.154776224C= GRCh38
NC_000023.10:g.154004499C= , CM000685.1:g.154004499C= GRCh37
NC_000023.9:g.153657693C= NCBI36
NG_009780.1:g.18469C= , LRG_55:g.18469C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.*172C= ENSP00000400542.2:n.*172C=
ENST00000426673.6:c.*818C= ENSP00000407253.3:n.*818C=
ENST00000484317.6:n.1650C=
ENST00000492372.2:n.314C=
ENST00000696575.1:c.1361C= ENSP00000512730.1:p.Pro454=
ENST00000696577.1:c.1376C= ENSP00000512731.1:p.Pro459=
ENST00000696578.1:c.*328C= ENSP00000512732.1:n.*328C=
ENST00000696579.1:n.2391C=
ENST00000696580.1:c.1289C= ENSP00000512733.1:p.Pro430=
ENST00000696581.1:c.*1350C= ENSP00000512734.1:n.*1350C=
ENST00000696582.1:c.*582C= ENSP00000512735.1:n.*582C=
ENST00000696583.1:c.1337C= ENSP00000512736.1:p.Pro446=
ENST00000696584.1:n.1900C=
ENST00000696585.1:n.2019C=
ENST00000696586.1:n.1793C=
ENST00000696587.1:c.1256C= ENSP00000512737.1:p.Pro419=
ENST00000696588.1:c.767C= ENSP00000513251.1:p.Pro256=
ENST00000696589.1:n.1151C=
ENST00000696590.1:n.2402C=
ENST00000696591.1:n.725C=
ENST00000696592.1:n.3657C=
ENST00000696627.1:c.*202C= ENSP00000512764.1:n.*202C=
ENST00000696628.1:c.1376C= ENSP00000512765.1:p.Pro459=
ENST00000369550.10:c.1376C= MANE Select ENSP00000358563.5:p.Pro459=
ENST00000369550.9:c.1376C= ENSP00000358563.5:p.Pro459=
ENST00000412124.5:c.634C=
ENST00000426673.5:c.795C=
ENST00000475966.1:n.865C=
ENST00000492372.1:n.193C=
ENST00000620277.4:c.*602C= ENSP00000478387.1:n.*602C=
NM_001142463.2:c.1361C= NP_001135935.1:p.Pro454=
NM_001288747.1:c.*602C= NP_001275676.1:n.*602C=
NM_001363.4:c.1376C= NP_001354.1:p.Pro459=
NR_110021.1:n.2077C=
NR_110022.1:n.2196C=
NR_110023.1:n.1970C=
NM_001363.5:c.1376C= MANE Select NP_001354.1:p.Pro459=
NM_001142463.3:c.1361C= NP_001135935.1:p.Pro454=
NR_110021.2:n.1955C=
NR_110022.2:n.2074C=
NR_110023.2:n.1848C=
NM_001288747.2:c.*602C= NP_001275676.1:n.*602C=