Canonical Allele Identifier: CA414895377

Gene: DKC1

Linked Data

• MyVariant Identifiers: chrX:g.154001465A>G (hg19) ; chrX:g.154773190A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773190A>G , CM000685.2:g.154773190A>G	GRCh38
NC_000023.10:g.154001465A>G , CM000685.1:g.154001465A>G	GRCh37
NC_000023.9:g.153654659A>G	NCBI36
NG_009780.1:g.15435A>G , LRG_55:g.15435A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.976A>G	ENSP00000400542.2:p.Ile326Val
ENST00000426673.6:c.*479A>G	ENSP00000407253.3:n.*479A>G
ENST00000484317.6:n.881A>G
ENST00000696575.1:c.1096A>G	ENSP00000512730.1:p.Ile366Val
ENST00000696577.1:c.1096A>G	ENSP00000512731.1:p.Ile366Val
ENST00000696578.1:c.*48A>G	ENSP00000512732.1:n.*48A>G
ENST00000696579.1:n.1198A>G
ENST00000696580.1:c.1009A>G	ENSP00000512733.1:p.Ile337Val
ENST00000696581.1:c.*1070A>G	ENSP00000512734.1:n.*1070A>G
ENST00000696582.1:c.*302A>G	ENSP00000512735.1:n.*302A>G
ENST00000696583.1:c.1057A>G	ENSP00000512736.1:p.Ile353Val
ENST00000696584.1:n.1620A>G
ENST00000696585.1:n.1739A>G
ENST00000696586.1:n.1513A>G
ENST00000696587.1:c.976A>G	ENSP00000512737.1:p.Ile326Val
ENST00000696588.1:c.487A>G	ENSP00000513251.1:p.Ile163Val
ENST00000696589.1:n.871A>G
ENST00000696590.1:n.720A>G
ENST00000696591.1:n.445A>G
ENST00000696592.1:n.1975A>G
ENST00000696627.1:c.1096A>G	ENSP00000512764.1:p.Ile366Val
ENST00000696628.1:c.1096A>G	ENSP00000512765.1:p.Ile366Val
ENST00000369550.10:c.1096A>G MANE Select	ENSP00000358563.5:p.Ile366Val
ENST00000369550.9:c.1096A>G	ENSP00000358563.5:p.Ile366Val
ENST00000412124.5:c.354A>G
ENST00000426673.5:c.456A>G
ENST00000475966.1:n.585A>G
ENST00000481062.1:n.47A>G
ENST00000620277.4:c.1096A>G	ENSP00000478387.1:p.Ile366Val
NM_001142463.2:c.1096A>G	NP_001135935.1:p.Ile366Val
NM_001288747.1:c.1096A>G	NP_001275676.1:p.Ile366Val
NM_001363.4:c.1096A>G	NP_001354.1:p.Ile366Val
NR_110021.1:n.1797A>G
NR_110022.1:n.1916A>G
NR_110023.1:n.1690A>G
NM_001363.5:c.1096A>G MANE Select	NP_001354.1:p.Ile366Val
NM_001142463.3:c.1096A>G	NP_001135935.1:p.Ile366Val
NR_110021.2:n.1675A>G
NR_110022.2:n.1794A>G
NR_110023.2:n.1568A>G
NM_001288747.2:c.1096A>G	NP_001275676.1:p.Ile366Val