Canonical Allele Identifier: CA414896014
Gene: DKC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154773222C>A , CM000685.2:g.154773222C>A GRCh38
NC_000023.10:g.154001497C>A , CM000685.1:g.154001497C>A GRCh37
NC_000023.9:g.153654691C>A NCBI36
NG_009780.1:g.15467C>A , LRG_55:g.15467C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.1008C>A ENSP00000400542.2:p.Tyr336Ter
ENST00000426673.6:c.*511C>A ENSP00000407253.3:n.*511C>A
ENST00000484317.6:n.913C>A
ENST00000696575.1:c.1128C>A ENSP00000512730.1:p.Tyr376Ter
ENST00000696577.1:c.1128C>A ENSP00000512731.1:p.Tyr376Ter
ENST00000696578.1:c.*80C>A ENSP00000512732.1:n.*80C>A
ENST00000696579.1:n.1230C>A
ENST00000696580.1:c.1041C>A ENSP00000512733.1:p.Tyr347Ter
ENST00000696581.1:c.*1102C>A ENSP00000512734.1:n.*1102C>A
ENST00000696582.1:c.*334C>A ENSP00000512735.1:n.*334C>A
ENST00000696583.1:c.1089C>A ENSP00000512736.1:p.Tyr363Ter
ENST00000696584.1:n.1652C>A
ENST00000696585.1:n.1771C>A
ENST00000696586.1:n.1545C>A
ENST00000696587.1:c.1008C>A ENSP00000512737.1:p.Tyr336Ter
ENST00000696588.1:c.519C>A ENSP00000513251.1:p.Tyr173Ter
ENST00000696589.1:n.903C>A
ENST00000696590.1:n.752C>A
ENST00000696591.1:n.477C>A
ENST00000696592.1:n.2007C>A
ENST00000696627.1:c.1128C>A ENSP00000512764.1:p.Tyr376Ter
ENST00000696628.1:c.1128C>A ENSP00000512765.1:p.Tyr376Ter
ENST00000369550.10:c.1128C>A MANE Select ENSP00000358563.5:p.Tyr376Ter
ENST00000369550.9:c.1128C>A ENSP00000358563.5:p.Tyr376Ter
ENST00000412124.5:c.386C>A
ENST00000426673.5:c.488C>A
ENST00000475966.1:n.617C>A
ENST00000481062.1:n.79C>A
ENST00000620277.4:c.1128C>A ENSP00000478387.1:p.Tyr376Ter
NM_001142463.2:c.1128C>A NP_001135935.1:p.Tyr376Ter
NM_001288747.1:c.1128C>A NP_001275676.1:p.Tyr376Ter
NM_001363.4:c.1128C>A NP_001354.1:p.Tyr376Ter
NR_110021.1:n.1829C>A
NR_110022.1:n.1948C>A
NR_110023.1:n.1722C>A
NM_001363.5:c.1128C>A MANE Select NP_001354.1:p.Tyr376Ter
NM_001142463.3:c.1128C>A NP_001135935.1:p.Tyr376Ter
NR_110021.2:n.1707C>A
NR_110022.2:n.1826C>A
NR_110023.2:n.1600C>A
NM_001288747.2:c.1128C>A NP_001275676.1:p.Tyr376Ter