Canonical Allele Identifier: CA414894999

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.154001420A>T (hg19) ; chrX:g.154773145A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773145A>T , CM000685.2:g.154773145A>T	GRCh38
NC_000023.10:g.154001420A>T , CM000685.1:g.154001420A>T	GRCh37
NC_000023.9:g.153654614A>T	NCBI36
NG_009780.1:g.15390A>T , LRG_55:g.15390A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000413910.6:c.931A>T	ENSP00000400542.2:p.Thr311Ser
ENST00000426673.6:c.*434A>T	ENSP00000407253.3:n.*434A>T
ENST00000484317.6:n.836A>T
ENST00000696575.1:c.1051A>T	ENSP00000512730.1:p.Thr351Ser
ENST00000696577.1:c.1051A>T	ENSP00000512731.1:p.Thr351Ser
ENST00000696578.1:c.*3A>T	ENSP00000512732.1:n.*3A>T
ENST00000696579.1:n.1153A>T
ENST00000696580.1:c.964A>T	ENSP00000512733.1:p.Thr322Ser
ENST00000696581.1:c.*1025A>T	ENSP00000512734.1:n.*1025A>T
ENST00000696582.1:c.*257A>T	ENSP00000512735.1:n.*257A>T
ENST00000696583.1:c.1012A>T	ENSP00000512736.1:p.Thr338Ser
ENST00000696584.1:n.1575A>T
ENST00000696585.1:n.1694A>T
ENST00000696586.1:n.1468A>T
ENST00000696587.1:c.931A>T	ENSP00000512737.1:p.Thr311Ser
ENST00000696588.1:c.442A>T	ENSP00000513251.1:p.Thr148Ser
ENST00000696589.1:n.826A>T
ENST00000696590.1:n.675A>T
ENST00000696591.1:n.400A>T
ENST00000696592.1:n.1930A>T
ENST00000696627.1:c.1051A>T	ENSP00000512764.1:p.Thr351Ser
ENST00000696628.1:c.1051A>T	ENSP00000512765.1:p.Thr351Ser
ENST00000369550.10:c.1051A>T MANE Select	ENSP00000358563.5:p.Thr351Ser
ENST00000369550.9:c.1051A>T	ENSP00000358563.5:p.Thr351Ser
ENST00000412124.5:c.309A>T
ENST00000426673.5:c.411A>T
ENST00000475966.1:n.540A>T
ENST00000481062.1:n.2A>T
ENST00000620277.4:c.1051A>T	ENSP00000478387.1:p.Thr351Ser
NM_001142463.2:c.1051A>T	NP_001135935.1:p.Thr351Ser
NM_001288747.1:c.1051A>T	NP_001275676.1:p.Thr351Ser
NM_001363.4:c.1051A>T	NP_001354.1:p.Thr351Ser
NR_110021.1:n.1752A>T
NR_110022.1:n.1871A>T
NR_110023.1:n.1645A>T
NM_001363.5:c.1051A>T MANE Select	NP_001354.1:p.Thr351Ser
NM_001142463.3:c.1051A>T	NP_001135935.1:p.Thr351Ser
NR_110021.2:n.1630A>T
NR_110022.2:n.1749A>T
NR_110023.2:n.1523A>T
NM_001288747.2:c.1051A>T	NP_001275676.1:p.Thr351Ser