Canonical Allele Identifier: CA341107

Gene: DKC1

Linked Data

• ClinVar Variation Id: 11582
• ClinVar RCV Id: RCV000012338
• dbSNP Id: rs121912293
• MyVariant Identifiers: chrX:g.153993740T>G (hg19) ; chrX:g.154765465T>G (hg38)
• PubMed: PMID:9042917 ; PMID:9590285 ; PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154765465T>G , CM000685.2:g.154765465T>G	GRCh38
NC_000023.10:g.153993740T>G , CM000685.1:g.153993740T>G	GRCh37
NC_000023.9:g.153646934T>G	NCBI36
NG_009780.1:g.7710T>G , LRG_55:g.7710T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.106T>G	ENSP00000400542.2:p.Phe36Val
ENST00000426673.6:c.106T>G	ENSP00000407253.3:p.Phe36Val
ENST00000696575.1:c.106T>G	ENSP00000512730.1:p.Phe36Val
ENST00000696576.1:n.208T>G
ENST00000696577.1:c.106T>G	ENSP00000512731.1:p.Phe36Val
ENST00000696578.1:c.106T>G	ENSP00000512732.1:p.Phe36Val
ENST00000696579.1:n.208T>G
ENST00000696580.1:c.85-442T>G	ENSP00000512733.1:n.85-442T>G
ENST00000696581.1:c.*80T>G	ENSP00000512734.1:n.*80T>G
ENST00000696582.1:c.106T>G	ENSP00000512735.1:p.Phe36Val
ENST00000696583.1:c.106T>G	ENSP00000512736.1:p.Phe36Val
ENST00000696584.1:n.630T>G
ENST00000696585.1:n.153T>G
ENST00000696586.1:n.153T>G
ENST00000696587.1:c.106T>G	ENSP00000512737.1:p.Phe36Val
ENST00000696588.1:c.-504T>G	ENSP00000513251.1:n.-504T>G
ENST00000696627.1:c.106T>G	ENSP00000512764.1:p.Phe36Val
ENST00000696628.1:c.106T>G	ENSP00000512765.1:p.Phe36Val
ENST00000369550.10:c.106T>G MANE Select	ENSP00000358563.5:p.Phe36Val
ENST00000369550.9:c.106T>G	ENSP00000358563.5:p.Phe36Val
ENST00000413910.5:c.106T>G	ENSP00000400542.1:p.Phe36Val
ENST00000437719.5:c.62T>G
ENST00000452771.5:c.64T>G	ENSP00000407325.1:p.Phe22Val
ENST00000473552.1:n.159T>G
ENST00000620277.4:c.106T>G	ENSP00000478387.1:p.Phe36Val
NM_001142463.2:c.106T>G	NP_001135935.1:p.Phe36Val
NM_001288747.1:c.106T>G	NP_001275676.1:p.Phe36Val
NM_001363.4:c.106T>G	NP_001354.1:p.Phe36Val
NR_110021.1:n.807T>G
NR_110022.1:n.330T>G
NR_110023.1:n.330T>G
NM_001363.5:c.106T>G MANE Select	NP_001354.1:p.Phe36Val
NM_001142463.3:c.106T>G	NP_001135935.1:p.Phe36Val
NR_110021.2:n.685T>G
NR_110022.2:n.208T>G
NR_110023.2:n.208T>G
NM_001288747.2:c.106T>G	NP_001275676.1:p.Phe36Val