Canonical Allele Identifier: CA2556033867

Gene: DKC1

Linked Data

• gnomAD v4: X-154773288-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154773288T>C , CM000685.2:g.154773288T>C	GRCh38
NC_000023.10:g.154001563T>C , CM000685.1:g.154001563T>C	GRCh37
NC_000023.9:g.153654757T>C	NCBI36
NG_009780.1:g.15533T>C , LRG_55:g.15533T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413910.6:c.1035+39T>C	ENSP00000400542.2:n.1035+39T>C
ENST00000426673.6:c.*538+39T>C	ENSP00000407253.3:n.*538+39T>C
ENST00000484317.6:n.940+39T>C
ENST00000696575.1:c.1155+39T>C	ENSP00000512730.1:n.1155+39T>C
ENST00000696577.1:c.1155+39T>C	ENSP00000512731.1:n.1155+39T>C
ENST00000696578.1:c.*107+39T>C	ENSP00000512732.1:n.*107+39T>C
ENST00000696579.1:n.1257+39T>C
ENST00000696580.1:c.1068+39T>C	ENSP00000512733.1:n.1068+39T>C
ENST00000696581.1:c.*1129+39T>C	ENSP00000512734.1:n.*1129+39T>C
ENST00000696582.1:c.*361+39T>C	ENSP00000512735.1:n.*361+39T>C
ENST00000696583.1:c.1116+39T>C	ENSP00000512736.1:n.1116+39T>C
ENST00000696584.1:n.1679+39T>C
ENST00000696585.1:n.1798+39T>C
ENST00000696586.1:n.1572+39T>C
ENST00000696587.1:c.1035+39T>C	ENSP00000512737.1:n.1035+39T>C
ENST00000696588.1:c.546+39T>C	ENSP00000513251.1:n.546+39T>C
ENST00000696589.1:n.930+39T>C
ENST00000696590.1:n.779+39T>C
ENST00000696591.1:n.504+39T>C
ENST00000696592.1:n.2034+39T>C
ENST00000696627.1:c.1159+35T>C	ENSP00000512764.1:n.1159+35T>C
ENST00000696628.1:c.1155+39T>C	ENSP00000512765.1:n.1155+39T>C
ENST00000369550.10:c.1155+39T>C MANE Select	ENSP00000358563.5:n.1155+39T>C
ENST00000369550.9:c.1155+39T>C	ENSP00000358563.5:n.1155+39T>C
ENST00000412124.5:c.413+39T>C
ENST00000426673.5:c.515+39T>C
ENST00000475966.1:n.644+39T>C
ENST00000481062.1:n.106+39T>C
ENST00000620277.4:c.1155+39T>C	ENSP00000478387.1:n.1155+39T>C
NM_001142463.2:c.1155+39T>C	NP_001135935.1:n.1155+39T>C
NM_001288747.1:c.1155+39T>C	NP_001275676.1:n.1155+39T>C
NM_001363.4:c.1155+39T>C	NP_001354.1:n.1155+39T>C
NR_110021.1:n.1856+39T>C
NR_110022.1:n.1975+39T>C
NR_110023.1:n.1749+39T>C
NM_001363.5:c.1155+39T>C MANE Select	NP_001354.1:n.1155+39T>C
NM_001142463.3:c.1155+39T>C	NP_001135935.1:n.1155+39T>C
NR_110021.2:n.1734+39T>C
NR_110022.2:n.1853+39T>C
NR_110023.2:n.1627+39T>C
NM_001288747.2:c.1155+39T>C	NP_001275676.1:n.1155+39T>C