Canonical Allele Identifier: CA519357809

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.154001437T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773162T>C , CM000685.2:g.154773162T>C	GRCh38
NC_000023.10:g.154001437T>C , CM000685.1:g.154001437T>C	GRCh37
NC_000023.9:g.153654631T>C	NCBI36
NG_009780.1:g.15407T>C , LRG_55:g.15407T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.948T>C	ENSP00000400542.2:p.Ser316=
ENST00000426673.6:c.*451T>C	ENSP00000407253.3:n.*451T>C
ENST00000484317.6:n.853T>C
ENST00000696575.1:c.1068T>C	ENSP00000512730.1:p.Ser356=
ENST00000696577.1:c.1068T>C	ENSP00000512731.1:p.Ser356=
ENST00000696578.1:c.*20T>C	ENSP00000512732.1:n.*20T>C
ENST00000696579.1:n.1170T>C
ENST00000696580.1:c.981T>C	ENSP00000512733.1:p.Ser327=
ENST00000696581.1:c.*1042T>C	ENSP00000512734.1:n.*1042T>C
ENST00000696582.1:c.*274T>C	ENSP00000512735.1:n.*274T>C
ENST00000696583.1:c.1029T>C	ENSP00000512736.1:p.Ser343=
ENST00000696584.1:n.1592T>C
ENST00000696585.1:n.1711T>C
ENST00000696586.1:n.1485T>C
ENST00000696587.1:c.948T>C	ENSP00000512737.1:p.Ser316=
ENST00000696588.1:c.459T>C	ENSP00000513251.1:p.Ser153=
ENST00000696589.1:n.843T>C
ENST00000696590.1:n.692T>C
ENST00000696591.1:n.417T>C
ENST00000696592.1:n.1947T>C
ENST00000696627.1:c.1068T>C	ENSP00000512764.1:p.Ser356=
ENST00000696628.1:c.1068T>C	ENSP00000512765.1:p.Ser356=
ENST00000369550.10:c.1068T>C MANE Select	ENSP00000358563.5:p.Ser356=
ENST00000369550.9:c.1068T>C	ENSP00000358563.5:p.Ser356=
ENST00000412124.5:c.326T>C
ENST00000426673.5:c.428T>C
ENST00000475966.1:n.557T>C
ENST00000481062.1:n.19T>C
ENST00000620277.4:c.1068T>C	ENSP00000478387.1:p.Ser356=
NM_001142463.2:c.1068T>C	NP_001135935.1:p.Ser356=
NM_001288747.1:c.1068T>C	NP_001275676.1:p.Ser356=
NM_001363.4:c.1068T>C	NP_001354.1:p.Ser356=
NR_110021.1:n.1769T>C
NR_110022.1:n.1888T>C
NR_110023.1:n.1662T>C
NM_001363.5:c.1068T>C MANE Select	NP_001354.1:p.Ser356=
NM_001142463.3:c.1068T>C	NP_001135935.1:p.Ser356=
NR_110021.2:n.1647T>C
NR_110022.2:n.1766T>C
NR_110023.2:n.1540T>C
NM_001288747.2:c.1068T>C	NP_001275676.1:p.Ser356=