Canonical Allele Identifier: CA414888744
Gene: DKC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154764938G>C , CM000685.2:g.154764938G>C GRCh38
NC_000023.10:g.153993213G>C , CM000685.1:g.153993213G>C GRCh37
NC_000023.9:g.153646407G>C NCBI36
NG_009780.1:g.7183G>C , LRG_55:g.7183G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000413910.6:c.56G>C ENSP00000400542.2:p.Arg19Pro
ENST00000426673.6:c.56G>C ENSP00000407253.3:p.Arg19Pro
ENST00000696575.1:c.56G>C ENSP00000512730.1:p.Arg19Pro
ENST00000696576.1:n.158G>C
ENST00000696577.1:c.56G>C ENSP00000512731.1:p.Arg19Pro
ENST00000696578.1:c.56G>C ENSP00000512732.1:p.Arg19Pro
ENST00000696579.1:n.158G>C
ENST00000696580.1:c.56G>C ENSP00000512733.1:p.Arg19Pro
ENST00000696581.1:c.56G>C ENSP00000512734.1:p.Arg19Pro
ENST00000696582.1:c.56G>C ENSP00000512735.1:p.Arg19Pro
ENST00000696583.1:c.56G>C ENSP00000512736.1:p.Arg19Pro
ENST00000696584.1:n.103G>C
ENST00000696585.1:n.103G>C
ENST00000696586.1:n.103G>C
ENST00000696587.1:c.56G>C ENSP00000512737.1:p.Arg19Pro
ENST00000696588.1:c.-1031G>C ENSP00000513251.1:n.-1031G>C
ENST00000696627.1:c.56G>C ENSP00000512764.1:p.Arg19Pro
ENST00000696628.1:c.56G>C ENSP00000512765.1:p.Arg19Pro
ENST00000369550.10:c.56G>C MANE Select ENSP00000358563.5:p.Arg19Pro
ENST00000369550.9:c.56G>C ENSP00000358563.5:p.Arg19Pro
ENST00000413910.5:c.56G>C ENSP00000400542.1:p.Arg19Pro
ENST00000437719.5:c.12G>C
ENST00000452771.5:c.14G>C ENSP00000407325.1:p.Arg5Pro
ENST00000473552.1:n.109G>C
ENST00000475423.1:n.170G>C
ENST00000620277.4:c.56G>C ENSP00000478387.1:p.Arg19Pro
NM_001142463.2:c.56G>C NP_001135935.1:p.Arg19Pro
NM_001288747.1:c.56G>C NP_001275676.1:p.Arg19Pro
NM_001363.4:c.56G>C NP_001354.1:p.Arg19Pro
NR_110021.1:n.280G>C
NR_110022.1:n.280G>C
NR_110023.1:n.280G>C
NM_001363.5:c.56G>C MANE Select NP_001354.1:p.Arg19Pro
NM_001142463.3:c.56G>C NP_001135935.1:p.Arg19Pro
NR_110021.2:n.158G>C
NR_110022.2:n.158G>C
NR_110023.2:n.158G>C
NM_001288747.2:c.56G>C NP_001275676.1:p.Arg19Pro