Canonical Allele Identifier: CA519357868
Gene: DKC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154001464G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154773189G>A , CM000685.2:g.154773189G>A GRCh38
NC_000023.10:g.154001464G>A , CM000685.1:g.154001464G>A GRCh37
NC_000023.9:g.153654658G>A NCBI36
NG_009780.1:g.15434G>A , LRG_55:g.15434G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.975G>A ENSP00000400542.2:p.Lys325=
ENST00000426673.6:c.*478G>A ENSP00000407253.3:n.*478G>A
ENST00000484317.6:n.880G>A
ENST00000696575.1:c.1095G>A ENSP00000512730.1:p.Lys365=
ENST00000696577.1:c.1095G>A ENSP00000512731.1:p.Lys365=
ENST00000696578.1:c.*47G>A ENSP00000512732.1:n.*47G>A
ENST00000696579.1:n.1197G>A
ENST00000696580.1:c.1008G>A ENSP00000512733.1:p.Lys336=
ENST00000696581.1:c.*1069G>A ENSP00000512734.1:n.*1069G>A
ENST00000696582.1:c.*301G>A ENSP00000512735.1:n.*301G>A
ENST00000696583.1:c.1056G>A ENSP00000512736.1:p.Lys352=
ENST00000696584.1:n.1619G>A
ENST00000696585.1:n.1738G>A
ENST00000696586.1:n.1512G>A
ENST00000696587.1:c.975G>A ENSP00000512737.1:p.Lys325=
ENST00000696588.1:c.486G>A ENSP00000513251.1:p.Lys162=
ENST00000696589.1:n.870G>A
ENST00000696590.1:n.719G>A
ENST00000696591.1:n.444G>A
ENST00000696592.1:n.1974G>A
ENST00000696627.1:c.1095G>A ENSP00000512764.1:p.Lys365=
ENST00000696628.1:c.1095G>A ENSP00000512765.1:p.Lys365=
ENST00000369550.10:c.1095G>A MANE Select ENSP00000358563.5:p.Lys365=
ENST00000369550.9:c.1095G>A ENSP00000358563.5:p.Lys365=
ENST00000412124.5:c.353G>A
ENST00000426673.5:c.455G>A
ENST00000475966.1:n.584G>A
ENST00000481062.1:n.46G>A
ENST00000620277.4:c.1095G>A ENSP00000478387.1:p.Lys365=
NM_001142463.2:c.1095G>A NP_001135935.1:p.Lys365=
NM_001288747.1:c.1095G>A NP_001275676.1:p.Lys365=
NM_001363.4:c.1095G>A NP_001354.1:p.Lys365=
NR_110021.1:n.1796G>A
NR_110022.1:n.1915G>A
NR_110023.1:n.1689G>A
NM_001363.5:c.1095G>A MANE Select NP_001354.1:p.Lys365=
NM_001142463.3:c.1095G>A NP_001135935.1:p.Lys365=
NR_110021.2:n.1674G>A
NR_110022.2:n.1793G>A
NR_110023.2:n.1567G>A
NM_001288747.2:c.1095G>A NP_001275676.1:p.Lys365=