Canonical Allele Identifier: CA2695161405

Gene: DKC1

Linked Data

• gnomAD v4: X-154773286-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773286_154773287insC , CM000685.2:g.154773286_154773287insC	GRCh38
NC_000023.10:g.154001561_154001562insC , CM000685.1:g.154001561_154001562insC	GRCh37
NC_000023.9:g.153654755_153654756insC	NCBI36
NG_009780.1:g.15531_15532insC , LRG_55:g.15531_15532insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.1035+37_1035+38insC	ENSP00000400542.2:n.1035+37_1035+38insC
ENST00000426673.6:c.*538+37_*538+38insC	ENSP00000407253.3:n.*538+37_*538+38insC
ENST00000484317.6:n.940+37_940+38insC
ENST00000696575.1:c.1155+37_1155+38insC	ENSP00000512730.1:n.1155+37_1155+38insC
ENST00000696577.1:c.1155+37_1155+38insC	ENSP00000512731.1:n.1155+37_1155+38insC
ENST00000696578.1:c.*107+37_*107+38insC	ENSP00000512732.1:n.*107+37_*107+38insC
ENST00000696579.1:n.1257+37_1257+38insC
ENST00000696580.1:c.1068+37_1068+38insC	ENSP00000512733.1:n.1068+37_1068+38insC
ENST00000696581.1:c.*1129+37_*1129+38insC	ENSP00000512734.1:n.*1129+37_*1129+38insC
ENST00000696582.1:c.*361+37_*361+38insC	ENSP00000512735.1:n.*361+37_*361+38insC
ENST00000696583.1:c.1116+37_1116+38insC	ENSP00000512736.1:n.1116+37_1116+38insC
ENST00000696584.1:n.1679+37_1679+38insC
ENST00000696585.1:n.1798+37_1798+38insC
ENST00000696586.1:n.1572+37_1572+38insC
ENST00000696587.1:c.1035+37_1035+38insC	ENSP00000512737.1:n.1035+37_1035+38insC
ENST00000696588.1:c.546+37_546+38insC	ENSP00000513251.1:n.546+37_546+38insC
ENST00000696589.1:n.930+37_930+38insC
ENST00000696590.1:n.779+37_779+38insC
ENST00000696591.1:n.504+37_504+38insC
ENST00000696592.1:n.2034+37_2034+38insC
ENST00000696627.1:c.1159+33_1159+34insC	ENSP00000512764.1:n.1159+33_1159+34insC
ENST00000696628.1:c.1155+37_1155+38insC	ENSP00000512765.1:n.1155+37_1155+38insC
ENST00000369550.10:c.1155+37_1155+38insC MANE Select	ENSP00000358563.5:n.1155+37_1155+38insC
ENST00000369550.9:c.1155+37_1155+38insC	ENSP00000358563.5:n.1155+37_1155+38insC
ENST00000412124.5:c.413+37_413+38insC
ENST00000426673.5:c.515+37_515+38insC
ENST00000475966.1:n.644+37_644+38insC
ENST00000481062.1:n.106+37_106+38insC
ENST00000620277.4:c.1155+37_1155+38insC	ENSP00000478387.1:n.1155+37_1155+38insC
NM_001142463.2:c.1155+37_1155+38insC	NP_001135935.1:n.1155+37_1155+38insC
NM_001288747.1:c.1155+37_1155+38insC	NP_001275676.1:n.1155+37_1155+38insC
NM_001363.4:c.1155+37_1155+38insC	NP_001354.1:n.1155+37_1155+38insC
NR_110021.1:n.1856+37_1856+38insC
NR_110022.1:n.1975+37_1975+38insC
NR_110023.1:n.1749+37_1749+38insC
NM_001363.5:c.1155+37_1155+38insC MANE Select	NP_001354.1:n.1155+37_1155+38insC
NM_001142463.3:c.1155+37_1155+38insC	NP_001135935.1:n.1155+37_1155+38insC
NR_110021.2:n.1734+37_1734+38insC
NR_110022.2:n.1853+37_1853+38insC
NR_110023.2:n.1627+37_1627+38insC
NM_001288747.2:c.1155+37_1155+38insC	NP_001275676.1:n.1155+37_1155+38insC