Canonical Allele Identifier: CA414895095

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.154001432A>G (hg19) ; chrX:g.154773157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773157A>G , CM000685.2:g.154773157A>G	GRCh38
NC_000023.10:g.154001432A>G , CM000685.1:g.154001432A>G	GRCh37
NC_000023.9:g.153654626A>G	NCBI36
NG_009780.1:g.15402A>G , LRG_55:g.15402A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000413910.6:c.943A>G	ENSP00000400542.2:p.Ile315Val
ENST00000426673.6:c.*446A>G	ENSP00000407253.3:n.*446A>G
ENST00000484317.6:n.848A>G
ENST00000696575.1:c.1063A>G	ENSP00000512730.1:p.Ile355Val
ENST00000696577.1:c.1063A>G	ENSP00000512731.1:p.Ile355Val
ENST00000696578.1:c.*15A>G	ENSP00000512732.1:n.*15A>G
ENST00000696579.1:n.1165A>G
ENST00000696580.1:c.976A>G	ENSP00000512733.1:p.Ile326Val
ENST00000696581.1:c.*1037A>G	ENSP00000512734.1:n.*1037A>G
ENST00000696582.1:c.*269A>G	ENSP00000512735.1:n.*269A>G
ENST00000696583.1:c.1024A>G	ENSP00000512736.1:p.Ile342Val
ENST00000696584.1:n.1587A>G
ENST00000696585.1:n.1706A>G
ENST00000696586.1:n.1480A>G
ENST00000696587.1:c.943A>G	ENSP00000512737.1:p.Ile315Val
ENST00000696588.1:c.454A>G	ENSP00000513251.1:p.Ile152Val
ENST00000696589.1:n.838A>G
ENST00000696590.1:n.687A>G
ENST00000696591.1:n.412A>G
ENST00000696592.1:n.1942A>G
ENST00000696627.1:c.1063A>G	ENSP00000512764.1:p.Ile355Val
ENST00000696628.1:c.1063A>G	ENSP00000512765.1:p.Ile355Val
ENST00000369550.10:c.1063A>G MANE Select	ENSP00000358563.5:p.Ile355Val
ENST00000369550.9:c.1063A>G	ENSP00000358563.5:p.Ile355Val
ENST00000412124.5:c.321A>G
ENST00000426673.5:c.423A>G
ENST00000475966.1:n.552A>G
ENST00000481062.1:n.14A>G
ENST00000620277.4:c.1063A>G	ENSP00000478387.1:p.Ile355Val
NM_001142463.2:c.1063A>G	NP_001135935.1:p.Ile355Val
NM_001288747.1:c.1063A>G	NP_001275676.1:p.Ile355Val
NM_001363.4:c.1063A>G	NP_001354.1:p.Ile355Val
NR_110021.1:n.1764A>G
NR_110022.1:n.1883A>G
NR_110023.1:n.1657A>G
NM_001363.5:c.1063A>G MANE Select	NP_001354.1:p.Ile355Val
NM_001142463.3:c.1063A>G	NP_001135935.1:p.Ile355Val
NR_110021.2:n.1642A>G
NR_110022.2:n.1761A>G
NR_110023.2:n.1535A>G
NM_001288747.2:c.1063A>G	NP_001275676.1:p.Ile355Val