Canonical Allele Identifier: CA414895069

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.154001429G>T (hg19) ; chrX:g.154773154G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773154G>T , CM000685.2:g.154773154G>T	GRCh38
NC_000023.10:g.154001429G>T , CM000685.1:g.154001429G>T	GRCh37
NC_000023.9:g.153654623G>T	NCBI36
NG_009780.1:g.15399G>T , LRG_55:g.15399G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000413910.6:c.940G>T	ENSP00000400542.2:p.Val314Phe
ENST00000426673.6:c.*443G>T	ENSP00000407253.3:n.*443G>T
ENST00000484317.6:n.845G>T
ENST00000696575.1:c.1060G>T	ENSP00000512730.1:p.Val354Phe
ENST00000696577.1:c.1060G>T	ENSP00000512731.1:p.Val354Phe
ENST00000696578.1:c.*12G>T	ENSP00000512732.1:n.*12G>T
ENST00000696579.1:n.1162G>T
ENST00000696580.1:c.973G>T	ENSP00000512733.1:p.Val325Phe
ENST00000696581.1:c.*1034G>T	ENSP00000512734.1:n.*1034G>T
ENST00000696582.1:c.*266G>T	ENSP00000512735.1:n.*266G>T
ENST00000696583.1:c.1021G>T	ENSP00000512736.1:p.Val341Phe
ENST00000696584.1:n.1584G>T
ENST00000696585.1:n.1703G>T
ENST00000696586.1:n.1477G>T
ENST00000696587.1:c.940G>T	ENSP00000512737.1:p.Val314Phe
ENST00000696588.1:c.451G>T	ENSP00000513251.1:p.Val151Phe
ENST00000696589.1:n.835G>T
ENST00000696590.1:n.684G>T
ENST00000696591.1:n.409G>T
ENST00000696592.1:n.1939G>T
ENST00000696627.1:c.1060G>T	ENSP00000512764.1:p.Val354Phe
ENST00000696628.1:c.1060G>T	ENSP00000512765.1:p.Val354Phe
ENST00000369550.10:c.1060G>T MANE Select	ENSP00000358563.5:p.Val354Phe
ENST00000369550.9:c.1060G>T	ENSP00000358563.5:p.Val354Phe
ENST00000412124.5:c.318G>T
ENST00000426673.5:c.420G>T
ENST00000475966.1:n.549G>T
ENST00000481062.1:n.11G>T
ENST00000620277.4:c.1060G>T	ENSP00000478387.1:p.Val354Phe
NM_001142463.2:c.1060G>T	NP_001135935.1:p.Val354Phe
NM_001288747.1:c.1060G>T	NP_001275676.1:p.Val354Phe
NM_001363.4:c.1060G>T	NP_001354.1:p.Val354Phe
NR_110021.1:n.1761G>T
NR_110022.1:n.1880G>T
NR_110023.1:n.1654G>T
NM_001363.5:c.1060G>T MANE Select	NP_001354.1:p.Val354Phe
NM_001142463.3:c.1060G>T	NP_001135935.1:p.Val354Phe
NR_110021.2:n.1639G>T
NR_110022.2:n.1758G>T
NR_110023.2:n.1532G>T
NM_001288747.2:c.1060G>T	NP_001275676.1:p.Val354Phe