Canonical Allele Identifier: CA2740090148

Gene: DKC1

Linked Data

• ClinVar Variation Id: 3020932
• ClinVar RCV Id: RCV003880091

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154769157del , CM000685.2:g.154769157del	GRCh38
NC_000023.10:g.153997432del , CM000685.1:g.153997432del	GRCh37
NC_000023.9:g.153650626del	NCBI36
NG_009780.1:g.11402del , LRG_55:g.11402del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.652-10del	ENSP00000400542.2:n.652-10del
ENST00000426673.6:c.*155-10del	ENSP00000407253.3:n.*155-10del
ENST00000484317.6:n.557-10del
ENST00000696575.1:c.772-10del	ENSP00000512730.1:n.772-10del
ENST00000696576.1:n.874-10del
ENST00000696577.1:c.772-10del	ENSP00000512731.1:n.772-10del
ENST00000696578.1:c.772-10del	ENSP00000512732.1:n.772-10del
ENST00000696579.1:n.874-10del
ENST00000696580.1:c.685-10del	ENSP00000512733.1:n.685-10del
ENST00000696581.1:c.*746-10del	ENSP00000512734.1:n.*746-10del
ENST00000696582.1:c.641-10del	ENSP00000512735.1:n.641-10del
ENST00000696583.1:c.772-49del	ENSP00000512736.1:n.772-49del
ENST00000696584.1:n.1296-10del
ENST00000696585.1:n.1415-10del
ENST00000696586.1:n.1189-10del
ENST00000696587.1:c.652-10del	ENSP00000512737.1:n.652-10del
ENST00000696588.1:c.163-10del	ENSP00000513251.1:n.163-10del
ENST00000696589.1:n.547-10del
ENST00000696590.1:n.396-10del
ENST00000696591.1:n.111del
ENST00000696627.1:c.772-10del	ENSP00000512764.1:n.772-10del
ENST00000696628.1:c.772-10del	ENSP00000512765.1:n.772-10del
ENST00000369550.10:c.772-10del MANE Select	ENSP00000358563.5:n.772-10del
ENST00000369550.9:c.772-10del	ENSP00000358563.5:n.772-10del
ENST00000412124.5:c.174-1602del
ENST00000413910.5:c.652-10del	ENSP00000400542.1:n.652-10del
ENST00000426673.5:c.132-10del
ENST00000452771.5:c.665-10del	ENSP00000407325.1:n.665-10del
ENST00000475966.1:n.261-10del
ENST00000484317.5:n.410-10del
ENST00000620277.4:c.772-10del	ENSP00000478387.1:n.772-10del
NM_001142463.2:c.772-10del	NP_001135935.1:n.772-10del
NM_001288747.1:c.772-10del	NP_001275676.1:n.772-10del
NM_001363.4:c.772-10del	NP_001354.1:n.772-10del
NR_110021.1:n.1473-10del
NR_110022.1:n.1592-10del
NR_110023.1:n.1366-10del
NM_001363.5:c.772-10del MANE Select	NP_001354.1:n.772-10del
NM_001142463.3:c.772-10del	NP_001135935.1:n.772-10del
NR_110021.2:n.1351-10del
NR_110022.2:n.1470-10del
NR_110023.2:n.1244-10del
NM_001288747.2:c.772-10del	NP_001275676.1:n.772-10del