Canonical Allele Identifier: CA2466784598
Gene: DKC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154765480G= , CM000685.2:g.154765480G= GRCh38
NC_000023.10:g.153993755G= , CM000685.1:g.153993755G= GRCh37
NC_000023.9:g.153646949G= NCBI36
NG_009780.1:g.7725G= , LRG_55:g.7725G=

Transcript Alleles

HGVS Amino-acid change
ENST00000413910.6:c.121G= ENSP00000400542.2:p.Glu41=
ENST00000426673.6:c.121G= ENSP00000407253.3:p.Glu41=
ENST00000696575.1:c.121G= ENSP00000512730.1:p.Glu41=
ENST00000696576.1:n.223G=
ENST00000696577.1:c.121G= ENSP00000512731.1:p.Glu41=
ENST00000696578.1:c.121G= ENSP00000512732.1:p.Glu41=
ENST00000696579.1:n.223G=
ENST00000696580.1:c.85-427G= ENSP00000512733.1:n.85-427G=
ENST00000696581.1:c.*95G= ENSP00000512734.1:n.*95G=
ENST00000696582.1:c.121G= ENSP00000512735.1:p.Glu41=
ENST00000696583.1:c.121G= ENSP00000512736.1:p.Glu41=
ENST00000696584.1:n.645G=
ENST00000696585.1:n.168G=
ENST00000696586.1:n.168G=
ENST00000696587.1:c.121G= ENSP00000512737.1:p.Glu41=
ENST00000696588.1:c.-489G= ENSP00000513251.1:n.-489G=
ENST00000696627.1:c.121G= ENSP00000512764.1:p.Glu41=
ENST00000696628.1:c.121G= ENSP00000512765.1:p.Glu41=
ENST00000369550.10:c.121G= MANE Select ENSP00000358563.5:p.Glu41=
ENST00000369550.9:c.121G= ENSP00000358563.5:p.Glu41=
ENST00000413910.5:c.121G= ENSP00000400542.1:p.Glu41=
ENST00000437719.5:c.77G=
ENST00000452771.5:c.79G= ENSP00000407325.1:p.Glu27=
ENST00000473552.1:n.174G=
ENST00000620277.4:c.121G= ENSP00000478387.1:p.Glu41=
NM_001142463.2:c.121G= NP_001135935.1:p.Glu41=
NM_001288747.1:c.121G= NP_001275676.1:p.Glu41=
NM_001363.4:c.121G= NP_001354.1:p.Glu41=
NR_110021.1:n.822G=
NR_110022.1:n.345G=
NR_110023.1:n.345G=
NM_001363.5:c.121G= MANE Select NP_001354.1:p.Glu41=
NM_001142463.3:c.121G= NP_001135935.1:p.Glu41=
NR_110021.2:n.700G=
NR_110022.2:n.223G=
NR_110023.2:n.223G=
NM_001288747.2:c.121G= NP_001275676.1:p.Glu41=