Canonical Allele Identifier: CA414895025

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.154001423A>T (hg19) ; chrX:g.154773148A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773148A>T , CM000685.2:g.154773148A>T	GRCh38
NC_000023.10:g.154001423A>T , CM000685.1:g.154001423A>T	GRCh37
NC_000023.9:g.153654617A>T	NCBI36
NG_009780.1:g.15393A>T , LRG_55:g.15393A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000413910.6:c.934A>T	ENSP00000400542.2:p.Thr312Ser
ENST00000426673.6:c.*437A>T	ENSP00000407253.3:n.*437A>T
ENST00000484317.6:n.839A>T
ENST00000696575.1:c.1054A>T	ENSP00000512730.1:p.Thr352Ser
ENST00000696577.1:c.1054A>T	ENSP00000512731.1:p.Thr352Ser
ENST00000696578.1:c.*6A>T	ENSP00000512732.1:n.*6A>T
ENST00000696579.1:n.1156A>T
ENST00000696580.1:c.967A>T	ENSP00000512733.1:p.Thr323Ser
ENST00000696581.1:c.*1028A>T	ENSP00000512734.1:n.*1028A>T
ENST00000696582.1:c.*260A>T	ENSP00000512735.1:n.*260A>T
ENST00000696583.1:c.1015A>T	ENSP00000512736.1:p.Thr339Ser
ENST00000696584.1:n.1578A>T
ENST00000696585.1:n.1697A>T
ENST00000696586.1:n.1471A>T
ENST00000696587.1:c.934A>T	ENSP00000512737.1:p.Thr312Ser
ENST00000696588.1:c.445A>T	ENSP00000513251.1:p.Thr149Ser
ENST00000696589.1:n.829A>T
ENST00000696590.1:n.678A>T
ENST00000696591.1:n.403A>T
ENST00000696592.1:n.1933A>T
ENST00000696627.1:c.1054A>T	ENSP00000512764.1:p.Thr352Ser
ENST00000696628.1:c.1054A>T	ENSP00000512765.1:p.Thr352Ser
ENST00000369550.10:c.1054A>T MANE Select	ENSP00000358563.5:p.Thr352Ser
ENST00000369550.9:c.1054A>T	ENSP00000358563.5:p.Thr352Ser
ENST00000412124.5:c.312A>T
ENST00000426673.5:c.414A>T
ENST00000475966.1:n.543A>T
ENST00000481062.1:n.5A>T
ENST00000620277.4:c.1054A>T	ENSP00000478387.1:p.Thr352Ser
NM_001142463.2:c.1054A>T	NP_001135935.1:p.Thr352Ser
NM_001288747.1:c.1054A>T	NP_001275676.1:p.Thr352Ser
NM_001363.4:c.1054A>T	NP_001354.1:p.Thr352Ser
NR_110021.1:n.1755A>T
NR_110022.1:n.1874A>T
NR_110023.1:n.1648A>T
NM_001363.5:c.1054A>T MANE Select	NP_001354.1:p.Thr352Ser
NM_001142463.3:c.1054A>T	NP_001135935.1:p.Thr352Ser
NR_110021.2:n.1633A>T
NR_110022.2:n.1752A>T
NR_110023.2:n.1526A>T
NM_001288747.2:c.1054A>T	NP_001275676.1:p.Thr352Ser