Canonical Allele Identifier: CA414895923

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.154001485G>C (hg19) ; chrX:g.154773210G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773210G>C , CM000685.2:g.154773210G>C	GRCh38
NC_000023.10:g.154001485G>C , CM000685.1:g.154001485G>C	GRCh37
NC_000023.9:g.153654679G>C	NCBI36
NG_009780.1:g.15455G>C , LRG_55:g.15455G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.996G>C	ENSP00000400542.2:p.Glu332Asp
ENST00000426673.6:c.*499G>C	ENSP00000407253.3:n.*499G>C
ENST00000484317.6:n.901G>C
ENST00000696575.1:c.1116G>C	ENSP00000512730.1:p.Glu372Asp
ENST00000696577.1:c.1116G>C	ENSP00000512731.1:p.Glu372Asp
ENST00000696578.1:c.*68G>C	ENSP00000512732.1:n.*68G>C
ENST00000696579.1:n.1218G>C
ENST00000696580.1:c.1029G>C	ENSP00000512733.1:p.Glu343Asp
ENST00000696581.1:c.*1090G>C	ENSP00000512734.1:n.*1090G>C
ENST00000696582.1:c.*322G>C	ENSP00000512735.1:n.*322G>C
ENST00000696583.1:c.1077G>C	ENSP00000512736.1:p.Glu359Asp
ENST00000696584.1:n.1640G>C
ENST00000696585.1:n.1759G>C
ENST00000696586.1:n.1533G>C
ENST00000696587.1:c.996G>C	ENSP00000512737.1:p.Glu332Asp
ENST00000696588.1:c.507G>C	ENSP00000513251.1:p.Glu169Asp
ENST00000696589.1:n.891G>C
ENST00000696590.1:n.740G>C
ENST00000696591.1:n.465G>C
ENST00000696592.1:n.1995G>C
ENST00000696627.1:c.1116G>C	ENSP00000512764.1:p.Glu372Asp
ENST00000696628.1:c.1116G>C	ENSP00000512765.1:p.Glu372Asp
ENST00000369550.10:c.1116G>C MANE Select	ENSP00000358563.5:p.Glu372Asp
ENST00000369550.9:c.1116G>C	ENSP00000358563.5:p.Glu372Asp
ENST00000412124.5:c.374G>C
ENST00000426673.5:c.476G>C
ENST00000475966.1:n.605G>C
ENST00000481062.1:n.67G>C
ENST00000620277.4:c.1116G>C	ENSP00000478387.1:p.Glu372Asp
NM_001142463.2:c.1116G>C	NP_001135935.1:p.Glu372Asp
NM_001288747.1:c.1116G>C	NP_001275676.1:p.Glu372Asp
NM_001363.4:c.1116G>C	NP_001354.1:p.Glu372Asp
NR_110021.1:n.1817G>C
NR_110022.1:n.1936G>C
NR_110023.1:n.1710G>C
NM_001363.5:c.1116G>C MANE Select	NP_001354.1:p.Glu372Asp
NM_001142463.3:c.1116G>C	NP_001135935.1:p.Glu372Asp
NR_110021.2:n.1695G>C
NR_110022.2:n.1814G>C
NR_110023.2:n.1588G>C
NM_001288747.2:c.1116G>C	NP_001275676.1:p.Glu372Asp