Canonical Allele Identifier: CA414891837

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.153997581G>C (hg19) ; chrX:g.154769306G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154769306G>C , CM000685.2:g.154769306G>C	GRCh38
NC_000023.10:g.153997581G>C , CM000685.1:g.153997581G>C	GRCh37
NC_000023.9:g.153650775G>C	NCBI36
NG_009780.1:g.11551G>C , LRG_55:g.11551G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.791G>C	ENSP00000400542.2:p.Ser264Thr
ENST00000426673.6:c.*294G>C	ENSP00000407253.3:n.*294G>C
ENST00000484317.6:n.696G>C
ENST00000696575.1:c.911G>C	ENSP00000512730.1:p.Ser304Thr
ENST00000696576.1:n.1013G>C
ENST00000696577.1:c.911G>C	ENSP00000512731.1:p.Ser304Thr
ENST00000696578.1:c.911G>C	ENSP00000512732.1:p.Ser304Thr
ENST00000696579.1:n.1013G>C
ENST00000696580.1:c.824G>C	ENSP00000512733.1:p.Ser275Thr
ENST00000696581.1:c.*885G>C	ENSP00000512734.1:n.*885G>C
ENST00000696582.1:c.*117G>C	ENSP00000512735.1:n.*117G>C
ENST00000696583.1:c.872G>C	ENSP00000512736.1:p.Ser291Thr
ENST00000696584.1:n.1435G>C
ENST00000696585.1:n.1554G>C
ENST00000696586.1:n.1328G>C
ENST00000696587.1:c.791G>C	ENSP00000512737.1:p.Ser264Thr
ENST00000696588.1:c.302G>C	ENSP00000513251.1:p.Ser101Thr
ENST00000696589.1:n.686G>C
ENST00000696590.1:n.535G>C
ENST00000696591.1:n.260G>C
ENST00000696627.1:c.911G>C	ENSP00000512764.1:p.Ser304Thr
ENST00000696628.1:c.911G>C	ENSP00000512765.1:p.Ser304Thr
ENST00000369550.10:c.911G>C MANE Select	ENSP00000358563.5:p.Ser304Thr
ENST00000369550.9:c.911G>C	ENSP00000358563.5:p.Ser304Thr
ENST00000412124.5:c.174-1453G>C
ENST00000426673.5:c.271G>C
ENST00000475966.1:n.400G>C
ENST00000484317.5:n.549G>C
ENST00000620277.4:c.911G>C	ENSP00000478387.1:p.Ser304Thr
NM_001142463.2:c.911G>C	NP_001135935.1:p.Ser304Thr
NM_001288747.1:c.911G>C	NP_001275676.1:p.Ser304Thr
NM_001363.4:c.911G>C	NP_001354.1:p.Ser304Thr
NR_110021.1:n.1612G>C
NR_110022.1:n.1731G>C
NR_110023.1:n.1505G>C
NM_001363.5:c.911G>C MANE Select	NP_001354.1:p.Ser304Thr
NM_001142463.3:c.911G>C	NP_001135935.1:p.Ser304Thr
NR_110021.2:n.1490G>C
NR_110022.2:n.1609G>C
NR_110023.2:n.1383G>C
NM_001288747.2:c.911G>C	NP_001275676.1:p.Ser304Thr