Canonical Allele Identifier: CA2695161373

Gene: DKC1

Linked Data

• gnomAD v4: X-154773281-G-GTTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773283_154773284insATTT , CM000685.2:g.154773283_154773284insATTT	GRCh38
NC_000023.10:g.154001558_154001559insATTT , CM000685.1:g.154001558_154001559insATTT	GRCh37
NC_000023.9:g.153654752_153654753insATTT	NCBI36
NG_009780.1:g.15528_15529insATTT , LRG_55:g.15528_15529insATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.1035+34_1035+35insATTT	ENSP00000400542.2:n.1035+34_1035+35insATTT
ENST00000426673.6:c.*538+34_*538+35insATTT	ENSP00000407253.3:n.*538+34_*538+35insATTT
ENST00000484317.6:n.940+34_940+35insATTT
ENST00000696575.1:c.1155+34_1155+35insATTT	ENSP00000512730.1:n.1155+34_1155+35insATTT
ENST00000696577.1:c.1155+34_1155+35insATTT	ENSP00000512731.1:n.1155+34_1155+35insATTT
ENST00000696578.1:c.*107+34_*107+35insATTT	ENSP00000512732.1:n.*107+34_*107+35insATTT
ENST00000696579.1:n.1257+34_1257+35insATTT
ENST00000696580.1:c.1068+34_1068+35insATTT	ENSP00000512733.1:n.1068+34_1068+35insATTT
ENST00000696581.1:c.*1129+34_*1129+35insATTT	ENSP00000512734.1:n.*1129+34_*1129+35insATTT
ENST00000696582.1:c.*361+34_*361+35insATTT	ENSP00000512735.1:n.*361+34_*361+35insATTT
ENST00000696583.1:c.1116+34_1116+35insATTT	ENSP00000512736.1:n.1116+34_1116+35insATTT
ENST00000696584.1:n.1679+34_1679+35insATTT
ENST00000696585.1:n.1798+34_1798+35insATTT
ENST00000696586.1:n.1572+34_1572+35insATTT
ENST00000696587.1:c.1035+34_1035+35insATTT	ENSP00000512737.1:n.1035+34_1035+35insATTT
ENST00000696588.1:c.546+34_546+35insATTT	ENSP00000513251.1:n.546+34_546+35insATTT
ENST00000696589.1:n.930+34_930+35insATTT
ENST00000696590.1:n.779+34_779+35insATTT
ENST00000696591.1:n.504+34_504+35insATTT
ENST00000696592.1:n.2034+34_2034+35insATTT
ENST00000696627.1:c.1159+30_1159+31insATTT	ENSP00000512764.1:n.1159+30_1159+31insATTT
ENST00000696628.1:c.1155+34_1155+35insATTT	ENSP00000512765.1:n.1155+34_1155+35insATTT
ENST00000369550.10:c.1155+34_1155+35insATTT MANE Select	ENSP00000358563.5:n.1155+34_1155+35insATTT
ENST00000369550.9:c.1155+34_1155+35insATTT	ENSP00000358563.5:n.1155+34_1155+35insATTT
ENST00000412124.5:c.413+34_413+35insATTT
ENST00000426673.5:c.515+34_515+35insATTT
ENST00000475966.1:n.644+34_644+35insATTT
ENST00000481062.1:n.106+34_106+35insATTT
ENST00000620277.4:c.1155+34_1155+35insATTT	ENSP00000478387.1:n.1155+34_1155+35insATTT
NM_001142463.2:c.1155+34_1155+35insATTT	NP_001135935.1:n.1155+34_1155+35insATTT
NM_001288747.1:c.1155+34_1155+35insATTT	NP_001275676.1:n.1155+34_1155+35insATTT
NM_001363.4:c.1155+34_1155+35insATTT	NP_001354.1:n.1155+34_1155+35insATTT
NR_110021.1:n.1856+34_1856+35insATTT
NR_110022.1:n.1975+34_1975+35insATTT
NR_110023.1:n.1749+34_1749+35insATTT
NM_001363.5:c.1155+34_1155+35insATTT MANE Select	NP_001354.1:n.1155+34_1155+35insATTT
NM_001142463.3:c.1155+34_1155+35insATTT	NP_001135935.1:n.1155+34_1155+35insATTT
NR_110021.2:n.1734+34_1734+35insATTT
NR_110022.2:n.1853+34_1853+35insATTT
NR_110023.2:n.1627+34_1627+35insATTT
NM_001288747.2:c.1155+34_1155+35insATTT	NP_001275676.1:n.1155+34_1155+35insATTT