Canonical Allele Identifier: CA2466787185

Gene: DKC1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773241G= , CM000685.2:g.154773241G=	GRCh38
NC_000023.10:g.154001516G= , CM000685.1:g.154001516G=	GRCh37
NC_000023.9:g.153654710G=	NCBI36
NG_009780.1:g.15486G= , LRG_55:g.15486G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.1027G=	ENSP00000400542.2:p.Gly343=
ENST00000426673.6:c.*530G=	ENSP00000407253.3:n.*530G=
ENST00000484317.6:n.932G=
ENST00000696575.1:c.1147G=	ENSP00000512730.1:p.Gly383=
ENST00000696577.1:c.1147G=	ENSP00000512731.1:p.Gly383=
ENST00000696578.1:c.*99G=	ENSP00000512732.1:n.*99G=
ENST00000696579.1:n.1249G=
ENST00000696580.1:c.1060G=	ENSP00000512733.1:p.Gly354=
ENST00000696581.1:c.*1121G=	ENSP00000512734.1:n.*1121G=
ENST00000696582.1:c.*353G=	ENSP00000512735.1:n.*353G=
ENST00000696583.1:c.1108G=	ENSP00000512736.1:p.Gly370=
ENST00000696584.1:n.1671G=
ENST00000696585.1:n.1790G=
ENST00000696586.1:n.1564G=
ENST00000696587.1:c.1027G=	ENSP00000512737.1:p.Gly343=
ENST00000696588.1:c.538G=	ENSP00000513251.1:p.Gly180=
ENST00000696589.1:n.922G=
ENST00000696590.1:n.771G=
ENST00000696591.1:n.496G=
ENST00000696592.1:n.2026G=
ENST00000696627.1:c.1147G=	ENSP00000512764.1:p.Gly383=
ENST00000696628.1:c.1147G=	ENSP00000512765.1:p.Gly383=
ENST00000369550.10:c.1147G= MANE Select	ENSP00000358563.5:p.Gly383=
ENST00000369550.9:c.1147G=	ENSP00000358563.5:p.Gly383=
ENST00000412124.5:c.405G=
ENST00000426673.5:c.507G=
ENST00000475966.1:n.636G=
ENST00000481062.1:n.98G=
ENST00000620277.4:c.1147G=	ENSP00000478387.1:p.Gly383=
NM_001142463.2:c.1147G=	NP_001135935.1:p.Gly383=
NM_001288747.1:c.1147G=	NP_001275676.1:p.Gly383=
NM_001363.4:c.1147G=	NP_001354.1:p.Gly383=
NR_110021.1:n.1848G=
NR_110022.1:n.1967G=
NR_110023.1:n.1741G=
NM_001363.5:c.1147G= MANE Select	NP_001354.1:p.Gly383=
NM_001142463.3:c.1147G=	NP_001135935.1:p.Gly383=
NR_110021.2:n.1726G=
NR_110022.2:n.1845G=
NR_110023.2:n.1619G=
NM_001288747.2:c.1147G=	NP_001275676.1:p.Gly383=