Canonical Allele Identifier: CA414891047

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.153997445C>A (hg19) ; chrX:g.154769170C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154769170C>A , CM000685.2:g.154769170C>A	GRCh38
NC_000023.10:g.153997445C>A , CM000685.1:g.153997445C>A	GRCh37
NC_000023.9:g.153650639C>A	NCBI36
NG_009780.1:g.11415C>A , LRG_55:g.11415C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.655C>A	ENSP00000400542.2:p.His219Asn
ENST00000426673.6:c.*158C>A	ENSP00000407253.3:n.*158C>A
ENST00000484317.6:n.560C>A
ENST00000696575.1:c.775C>A	ENSP00000512730.1:p.His259Asn
ENST00000696576.1:n.877C>A
ENST00000696577.1:c.775C>A	ENSP00000512731.1:p.His259Asn
ENST00000696578.1:c.775C>A	ENSP00000512732.1:p.His259Asn
ENST00000696579.1:n.877C>A
ENST00000696580.1:c.688C>A	ENSP00000512733.1:p.His230Asn
ENST00000696581.1:c.*749C>A	ENSP00000512734.1:n.*749C>A
ENST00000696582.1:c.644C>A	ENSP00000512735.1:p.Pro215Gln
ENST00000696583.1:c.772-36C>A	ENSP00000512736.1:n.772-36C>A
ENST00000696584.1:n.1299C>A
ENST00000696585.1:n.1418C>A
ENST00000696586.1:n.1192C>A
ENST00000696587.1:c.655C>A	ENSP00000512737.1:p.His219Asn
ENST00000696588.1:c.166C>A	ENSP00000513251.1:p.His56Asn
ENST00000696589.1:n.550C>A
ENST00000696590.1:n.399C>A
ENST00000696591.1:n.124C>A
ENST00000696627.1:c.775C>A	ENSP00000512764.1:p.His259Asn
ENST00000696628.1:c.775C>A	ENSP00000512765.1:p.His259Asn
ENST00000369550.10:c.775C>A MANE Select	ENSP00000358563.5:p.His259Asn
ENST00000369550.9:c.775C>A	ENSP00000358563.5:p.His259Asn
ENST00000412124.5:c.174-1589C>A
ENST00000413910.5:c.655C>A	ENSP00000400542.1:p.His219Asn
ENST00000426673.5:c.135C>A
ENST00000452771.5:c.668C>A	ENSP00000407325.1:n.668C>A
ENST00000475966.1:n.264C>A
ENST00000484317.5:n.413C>A
ENST00000620277.4:c.775C>A	ENSP00000478387.1:p.His259Asn
NM_001142463.2:c.775C>A	NP_001135935.1:p.His259Asn
NM_001288747.1:c.775C>A	NP_001275676.1:p.His259Asn
NM_001363.4:c.775C>A	NP_001354.1:p.His259Asn
NR_110021.1:n.1476C>A
NR_110022.1:n.1595C>A
NR_110023.1:n.1369C>A
NM_001363.5:c.775C>A MANE Select	NP_001354.1:p.His259Asn
NM_001142463.3:c.775C>A	NP_001135935.1:p.His259Asn
NR_110021.2:n.1354C>A
NR_110022.2:n.1473C>A
NR_110023.2:n.1247C>A
NM_001288747.2:c.775C>A	NP_001275676.1:p.His259Asn