Canonical Allele Identifier: CA414895277

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.154001451G>A (hg19) ; chrX:g.154773176G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773176G>A , CM000685.2:g.154773176G>A	GRCh38
NC_000023.10:g.154001451G>A , CM000685.1:g.154001451G>A	GRCh37
NC_000023.9:g.153654645G>A	NCBI36
NG_009780.1:g.15421G>A , LRG_55:g.15421G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.962G>A	ENSP00000400542.2:p.Gly321Asp
ENST00000426673.6:c.*465G>A	ENSP00000407253.3:n.*465G>A
ENST00000484317.6:n.867G>A
ENST00000696575.1:c.1082G>A	ENSP00000512730.1:p.Gly361Asp
ENST00000696577.1:c.1082G>A	ENSP00000512731.1:p.Gly361Asp
ENST00000696578.1:c.*34G>A	ENSP00000512732.1:n.*34G>A
ENST00000696579.1:n.1184G>A
ENST00000696580.1:c.995G>A	ENSP00000512733.1:p.Gly332Asp
ENST00000696581.1:c.*1056G>A	ENSP00000512734.1:n.*1056G>A
ENST00000696582.1:c.*288G>A	ENSP00000512735.1:n.*288G>A
ENST00000696583.1:c.1043G>A	ENSP00000512736.1:p.Gly348Asp
ENST00000696584.1:n.1606G>A
ENST00000696585.1:n.1725G>A
ENST00000696586.1:n.1499G>A
ENST00000696587.1:c.962G>A	ENSP00000512737.1:p.Gly321Asp
ENST00000696588.1:c.473G>A	ENSP00000513251.1:p.Gly158Asp
ENST00000696589.1:n.857G>A
ENST00000696590.1:n.706G>A
ENST00000696591.1:n.431G>A
ENST00000696592.1:n.1961G>A
ENST00000696627.1:c.1082G>A	ENSP00000512764.1:p.Gly361Asp
ENST00000696628.1:c.1082G>A	ENSP00000512765.1:p.Gly361Asp
ENST00000369550.10:c.1082G>A MANE Select	ENSP00000358563.5:p.Gly361Asp
ENST00000369550.9:c.1082G>A	ENSP00000358563.5:p.Gly361Asp
ENST00000412124.5:c.340G>A
ENST00000426673.5:c.442G>A
ENST00000475966.1:n.571G>A
ENST00000481062.1:n.33G>A
ENST00000620277.4:c.1082G>A	ENSP00000478387.1:p.Gly361Asp
NM_001142463.2:c.1082G>A	NP_001135935.1:p.Gly361Asp
NM_001288747.1:c.1082G>A	NP_001275676.1:p.Gly361Asp
NM_001363.4:c.1082G>A	NP_001354.1:p.Gly361Asp
NR_110021.1:n.1783G>A
NR_110022.1:n.1902G>A
NR_110023.1:n.1676G>A
NM_001363.5:c.1082G>A MANE Select	NP_001354.1:p.Gly361Asp
NM_001142463.3:c.1082G>A	NP_001135935.1:p.Gly361Asp
NR_110021.2:n.1661G>A
NR_110022.2:n.1780G>A
NR_110023.2:n.1554G>A
NM_001288747.2:c.1082G>A	NP_001275676.1:p.Gly361Asp