Canonical Allele Identifier: CA2466787182

Gene: DKC1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773226C= , CM000685.2:g.154773226C=	GRCh38
NC_000023.10:g.154001501C= , CM000685.1:g.154001501C=	GRCh37
NC_000023.9:g.153654695C=	NCBI36
NG_009780.1:g.15471C= , LRG_55:g.15471C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.1012C=	ENSP00000400542.2:p.Arg338=
ENST00000426673.6:c.*515C=	ENSP00000407253.3:n.*515C=
ENST00000484317.6:n.917C=
ENST00000696575.1:c.1132C=	ENSP00000512730.1:p.Arg378=
ENST00000696577.1:c.1132C=	ENSP00000512731.1:p.Arg378=
ENST00000696578.1:c.*84C=	ENSP00000512732.1:n.*84C=
ENST00000696579.1:n.1234C=
ENST00000696580.1:c.1045C=	ENSP00000512733.1:p.Arg349=
ENST00000696581.1:c.*1106C=	ENSP00000512734.1:n.*1106C=
ENST00000696582.1:c.*338C=	ENSP00000512735.1:n.*338C=
ENST00000696583.1:c.1093C=	ENSP00000512736.1:p.Arg365=
ENST00000696584.1:n.1656C=
ENST00000696585.1:n.1775C=
ENST00000696586.1:n.1549C=
ENST00000696587.1:c.1012C=	ENSP00000512737.1:p.Arg338=
ENST00000696588.1:c.523C=	ENSP00000513251.1:p.Arg175=
ENST00000696589.1:n.907C=
ENST00000696590.1:n.756C=
ENST00000696591.1:n.481C=
ENST00000696592.1:n.2011C=
ENST00000696627.1:c.1132C=	ENSP00000512764.1:p.Arg378=
ENST00000696628.1:c.1132C=	ENSP00000512765.1:p.Arg378=
ENST00000369550.10:c.1132C= MANE Select	ENSP00000358563.5:p.Arg378=
ENST00000369550.9:c.1132C=	ENSP00000358563.5:p.Arg378=
ENST00000412124.5:c.390C=
ENST00000426673.5:c.492C=
ENST00000475966.1:n.621C=
ENST00000481062.1:n.83C=
ENST00000620277.4:c.1132C=	ENSP00000478387.1:p.Arg378=
NM_001142463.2:c.1132C=	NP_001135935.1:p.Arg378=
NM_001288747.1:c.1132C=	NP_001275676.1:p.Arg378=
NM_001363.4:c.1132C=	NP_001354.1:p.Arg378=
NR_110021.1:n.1833C=
NR_110022.1:n.1952C=
NR_110023.1:n.1726C=
NM_001363.5:c.1132C= MANE Select	NP_001354.1:p.Arg378=
NM_001142463.3:c.1132C=	NP_001135935.1:p.Arg378=
NR_110021.2:n.1711C=
NR_110022.2:n.1830C=
NR_110023.2:n.1604C=
NM_001288747.2:c.1132C=	NP_001275676.1:p.Arg378=