Canonical Allele Identifier: CA645246627

Gene: DKC1

Linked Data

• dbSNP Id: rs1397760652
• gnomAD v2: X-153993574-TTC-T
• gnomAD v3: X-154765299-TTC-T
• gnomAD v4: X-154765299-TTC-T
• MyVariant Identifiers: chrX:g.153993575_153993576del (hg19) ; chrX:g.154765300_154765301del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154765307_154765308del , CM000685.2:g.154765307_154765308del	GRCh38
NC_000023.10:g.153993582_153993583del , CM000685.1:g.153993582_153993583del	GRCh37
NC_000023.9:g.153646776_153646777del	NCBI36
NG_009780.1:g.7552_7553del , LRG_55:g.7552_7553del

Transcript Alleles

HGVS	Amino-acid change
ENST00000413910.6:c.85-137_85-136del	ENSP00000400542.2:n.85-137_85-136del
ENST00000426673.6:c.85-137_85-136del	ENSP00000407253.3:n.85-137_85-136del
ENST00000696575.1:c.85-137_85-136del	ENSP00000512730.1:n.85-137_85-136del
ENST00000696576.1:n.187-137_187-136del
ENST00000696577.1:c.85-137_85-136del	ENSP00000512731.1:n.85-137_85-136del
ENST00000696578.1:c.85-137_85-136del	ENSP00000512732.1:n.85-137_85-136del
ENST00000696579.1:n.187-137_187-136del
ENST00000696580.1:c.84+341_84+342del	ENSP00000512733.1:n.84+341_84+342del
ENST00000696581.1:c.85-13_85-12del	ENSP00000512734.1:n.85-13_85-12del
ENST00000696582.1:c.85-137_85-136del	ENSP00000512735.1:n.85-137_85-136del
ENST00000696583.1:c.85-137_85-136del	ENSP00000512736.1:n.85-137_85-136del
ENST00000696584.1:n.472_473del
ENST00000696585.1:n.132-137_132-136del
ENST00000696586.1:n.132-137_132-136del
ENST00000696587.1:c.85-137_85-136del	ENSP00000512737.1:n.85-137_85-136del
ENST00000696588.1:c.-662_-661del	ENSP00000513251.1:n.-662_-661del
ENST00000696627.1:c.85-137_85-136del	ENSP00000512764.1:n.85-137_85-136del
ENST00000696628.1:c.85-137_85-136del	ENSP00000512765.1:n.85-137_85-136del
ENST00000369550.10:c.85-137_85-136del MANE Select	ENSP00000358563.5:n.85-137_85-136del
ENST00000369550.9:c.85-137_85-136del	ENSP00000358563.5:n.85-137_85-136del
ENST00000413910.5:c.85-137_85-136del	ENSP00000400542.1:n.85-137_85-136del
ENST00000437719.5:c.41-137_41-136del
ENST00000452771.5:c.43-137_43-136del	ENSP00000407325.1:n.43-137_43-136del
ENST00000473552.1:n.138-137_138-136del
ENST00000475423.1:n.539_540del
ENST00000620277.4:c.85-137_85-136del	ENSP00000478387.1:n.85-137_85-136del
NM_001142463.2:c.85-137_85-136del	NP_001135935.1:n.85-137_85-136del
NM_001288747.1:c.85-137_85-136del	NP_001275676.1:n.85-137_85-136del
NM_001363.4:c.85-137_85-136del	NP_001354.1:n.85-137_85-136del
NR_110021.1:n.649_650del
NR_110022.1:n.309-137_309-136del
NR_110023.1:n.309-137_309-136del
NM_001363.5:c.85-137_85-136del MANE Select	NP_001354.1:n.85-137_85-136del
NM_001142463.3:c.85-137_85-136del	NP_001135935.1:n.85-137_85-136del
NR_110021.2:n.527_528del
NR_110022.2:n.187-137_187-136del
NR_110023.2:n.187-137_187-136del
NM_001288747.2:c.85-137_85-136del	NP_001275676.1:n.85-137_85-136del