Canonical Allele Identifier: CA2466787132
Gene: DKC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154773072C= , CM000685.2:g.154773072C= GRCh38
NC_000023.10:g.154001347C= , CM000685.1:g.154001347C= GRCh37
NC_000023.9:g.153654541C= NCBI36
NG_009780.1:g.15317C= , LRG_55:g.15317C=

Transcript Alleles

HGVS Amino-acid change
ENST00000413910.6:c.917-59C= ENSP00000400542.2:n.917-59C=
ENST00000426673.6:c.*420-59C= ENSP00000407253.3:n.*420-59C=
ENST00000484317.6:n.822-59C=
ENST00000696575.1:c.1037-59C= ENSP00000512730.1:n.1037-59C=
ENST00000696577.1:c.1037-59C= ENSP00000512731.1:n.1037-59C=
ENST00000696578.1:c.916-59C= ENSP00000512732.1:n.916-59C=
ENST00000696579.1:n.1139-59C=
ENST00000696580.1:c.950-59C= ENSP00000512733.1:n.950-59C=
ENST00000696581.1:c.*1011-59C= ENSP00000512734.1:n.*1011-59C=
ENST00000696582.1:c.*243-59C= ENSP00000512735.1:n.*243-59C=
ENST00000696583.1:c.998-59C= ENSP00000512736.1:n.998-59C=
ENST00000696584.1:n.1561-59C=
ENST00000696585.1:n.1680-59C=
ENST00000696586.1:n.1454-59C=
ENST00000696587.1:c.917-59C= ENSP00000512737.1:n.917-59C=
ENST00000696588.1:c.428-59C= ENSP00000513251.1:n.428-59C=
ENST00000696589.1:n.812-59C=
ENST00000696590.1:n.661-59C=
ENST00000696591.1:n.386-59C=
ENST00000696592.1:n.1857C=
ENST00000696627.1:c.1037-59C= ENSP00000512764.1:n.1037-59C=
ENST00000696628.1:c.1037-59C= ENSP00000512765.1:n.1037-59C=
ENST00000369550.10:c.1037-59C= MANE Select ENSP00000358563.5:n.1037-59C=
ENST00000369550.9:c.1037-59C= ENSP00000358563.5:n.1037-59C=
ENST00000412124.5:c.295-59C=
ENST00000426673.5:c.397-59C=
ENST00000475966.1:n.526-59C=
ENST00000620277.4:c.1037-59C= ENSP00000478387.1:n.1037-59C=
NM_001142463.2:c.1037-59C= NP_001135935.1:n.1037-59C=
NM_001288747.1:c.1037-59C= NP_001275676.1:n.1037-59C=
NM_001363.4:c.1037-59C= NP_001354.1:n.1037-59C=
NR_110021.1:n.1738-59C=
NR_110022.1:n.1857-59C=
NR_110023.1:n.1631-59C=
NM_001363.5:c.1037-59C= MANE Select NP_001354.1:n.1037-59C=
NM_001142463.3:c.1037-59C= NP_001135935.1:n.1037-59C=
NR_110021.2:n.1616-59C=
NR_110022.2:n.1735-59C=
NR_110023.2:n.1509-59C=
NM_001288747.2:c.1037-59C= NP_001275676.1:n.1037-59C=