Canonical Allele Identifier: CA10590090
Gene: CYLD HGNC NCBI
CYLD-AS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 267253
ClinVar RCV Id: RCV000257939
dbSNP Id: rs886040892

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50793601_50793602del , CM000678.2:g.50793601_50793602del GRCh38
NC_000016.9:g.50827512_50827513del , CM000678.1:g.50827512_50827513del GRCh37
NC_000016.8:g.49385013_49385014del NCBI36
NG_012061.1:g.56552_56553del , LRG_491:g.56552_56553del

Transcript Alleles

HGVS Amino-acid change
ENST00000427738.8:c.2406_2407del (CYLD) MANE Select ENSP00000392025.3:p.Cys802Ter
ENST00000311559.13:c.2406_2407del (CYLD) ENSP00000308928.9:p.Cys802Ter
ENST00000398568.6:c.2397_2398del (CYLD) ENSP00000381574.2:p.Cys799Ter
ENST00000427738.7:c.2406_2407del (CYLD) ENSP00000392025.3:p.Cys802Ter
ENST00000564326.5:c.2397_2398del (CYLD) ENSP00000454515.1:p.Cys799Ter
ENST00000566206.5:c.2397_2398del (CYLD) ENSP00000462134.1:p.Cys799Ter
ENST00000568704.2:c.1851_1852del (CYLD) ENSP00000456488.2:p.Cys617Ter
ENST00000569418.5:c.2397_2398del (CYLD) ENSP00000457576.1:p.Cys799Ter
NM_001042355.1:c.2397_2398del (CYLD) NP_001035814.1:p.Cys799Ter
NM_001042412.1:c.2397_2398del (CYLD) NP_001035877.1:p.Cys799Ter
NM_015247.2:c.2406_2407del , LRG_491t1:c.2406_2407del (CYLD) NP_056062.1:p.Cys802Ter
XM_005255812.2:c.2397_2398del (CYLD) XP_005255869.1:p.Cys799Ter
XM_006721149.1:c.2397_2398del (CYLD) XP_006721212.1:p.Cys799Ter
XM_011522906.1:c.2397_2398del (CYLD) XP_011521208.1:p.Cys799Ter
XM_011522907.1:c.2397_2398del (CYLD) XP_011521209.1:p.Cys799Ter
XM_011522908.1:c.2367_2368del (CYLD) XP_011521210.1:p.Cys789Ter
XM_011522909.1:c.2397_2398del (CYLD) XP_011521211.1:p.Cys799Ter
XM_011522910.1:c.2397_2398del (CYLD) XP_011521212.1:p.Cys799Ter
XR_933218.1:n.2690_2691del (CYLD)
XR_933542.1:n.2450+8521_2450+8522del (CYLD-AS2)
XM_011522907.2:c.2397_2398del (CYLD) XP_011521209.1:p.Cys799Ter
XM_017022977.1:c.2397_2398del (CYLD) XP_016878466.1:p.Cys799Ter
XM_017022978.1:c.2397_2398del (CYLD) XP_016878467.1:p.Cys799Ter
XM_017022979.1:c.2397_2398del (CYLD) XP_016878468.1:p.Cys799Ter
XM_017022980.1:c.2397_2398del (CYLD) XP_016878469.1:p.Cys799Ter
XM_017022981.2:c.2367_2368del (CYLD) XP_016878470.1:p.Cys789Ter
XR_001751849.1:n.2524_2525del (CYLD)
XR_933542.2:n.4187+8521_4187+8522del (CYLD-AS2)
NM_001042355.2:c.2397_2398del (CYLD) NP_001035814.1:p.Cys799Ter
NM_001042412.2:c.2397_2398del (CYLD) NP_001035877.1:p.Cys799Ter
NM_001042412.3:c.2397_2398del (CYLD) NP_001035877.1:p.Cys799Ter
NM_001378743.1:c.2406_2407del (CYLD) MANE Select NP_001365672.1:p.Cys802Ter
NM_001378744.1:c.2397_2398del (CYLD) NP_001365673.1:p.Cys799Ter
NM_001378745.1:c.2397_2398del (CYLD) NP_001365674.1:p.Cys799Ter
NM_001378746.1:c.2397_2398del (CYLD) NP_001365675.1:p.Cys799Ter
NM_001378747.1:c.2397_2398del (CYLD) NP_001365676.1:p.Cys799Ter
NM_001378748.1:c.2397_2398del (CYLD) NP_001365677.1:p.Cys799Ter
NM_001378749.1:c.2397_2398del (CYLD) NP_001365678.1:p.Cys799Ter
NM_001378750.1:c.2397_2398del (CYLD) NP_001365679.1:p.Cys799Ter
NM_001378751.1:c.2367_2368del (CYLD) NP_001365680.1:p.Cys789Ter
NM_001378752.1:c.2367_2368del (CYLD) NP_001365681.1:p.Cys789Ter
NM_001378753.1:c.2367_2368del (CYLD) NP_001365682.1:p.Cys789Ter
NM_001378754.1:c.1731_1732del (CYLD) NP_001365683.1:p.Cys577Ter
NM_001378755.1:c.1731_1732del (CYLD) NP_001365684.1:p.Cys577Ter
NM_015247.3:c.2406_2407del (CYLD) NP_056062.1:p.Cys802Ter
NR_166071.1:n.2495_2496del (CYLD)