Canonical Allele Identifier: CA395886081

Gene: CYLD CYLD-AS2

Linked Data

• dbSNP Id: rs2151047774
• COSMIC: COSM4675856
• MyVariant Identifiers: chr16:g.50830349G>A (hg19) ; chr16:g.50796438G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50796438G>A , CM000678.2:g.50796438G>A	GRCh38
NC_000016.9:g.50830349G>A , CM000678.1:g.50830349G>A	GRCh37
NC_000016.8:g.49387850G>A	NCBI36
NG_012061.1:g.59389G>A , LRG_491:g.59389G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427738.8:c.2801G>A (CYLD) MANE Select	ENSP00000392025.3:p.Cys934Tyr
ENST00000311559.13:c.2801G>A (CYLD)	ENSP00000308928.9:p.Cys934Tyr
ENST00000398568.6:c.2792G>A (CYLD)	ENSP00000381574.2:p.Cys931Tyr
ENST00000427738.7:c.2801G>A (CYLD)	ENSP00000392025.3:p.Cys934Tyr
ENST00000564326.5:c.2792G>A (CYLD)	ENSP00000454515.1:p.Cys931Tyr
ENST00000566024.1:c.177+1968G>A (CYLD)
ENST00000568704.2:c.2246G>A (CYLD)	ENSP00000456488.2:p.Cys749Tyr
ENST00000569418.5:c.2792G>A (CYLD)	ENSP00000457576.1:p.Cys931Tyr
NM_001042355.1:c.2792G>A (CYLD)	NP_001035814.1:p.Cys931Tyr
NM_001042412.1:c.2792G>A (CYLD)	NP_001035877.1:p.Cys931Tyr
NM_015247.2:c.2801G>A , LRG_491t1:c.2801G>A (CYLD)	NP_056062.1:p.Cys934Tyr
XM_005255812.2:c.2792G>A (CYLD)	XP_005255869.1:p.Cys931Tyr
XM_006721149.1:c.2792G>A (CYLD)	XP_006721212.1:p.Cys931Tyr
XM_011522906.1:c.2792G>A (CYLD)	XP_011521208.1:p.Cys931Tyr
XM_011522907.1:c.2792G>A (CYLD)	XP_011521209.1:p.Cys931Tyr
XM_011522908.1:c.2762G>A (CYLD)	XP_011521210.1:p.Cys921Tyr
XM_011522909.1:c.2677+2010G>A (CYLD)	XP_011521211.1:n.2677+2010G>A
XM_011522910.1:c.2677+2010G>A (CYLD)	XP_011521212.1:n.2677+2010G>A
XR_933218.1:n.3085G>A (CYLD)
XR_933542.1:n.2450+5685C>T (CYLD-AS2)
XM_011522907.2:c.2792G>A (CYLD)	XP_011521209.1:p.Cys931Tyr
XM_017022977.1:c.2792G>A (CYLD)	XP_016878466.1:p.Cys931Tyr
XM_017022978.1:c.2792G>A (CYLD)	XP_016878467.1:p.Cys931Tyr
XM_017022979.1:c.2792G>A (CYLD)	XP_016878468.1:p.Cys931Tyr
XM_017022980.1:c.2792G>A (CYLD)	XP_016878469.1:p.Cys931Tyr
XM_017022981.2:c.2762G>A (CYLD)	XP_016878470.1:p.Cys921Tyr
XR_001751849.1:n.2919G>A (CYLD)
XR_933542.2:n.4187+5685C>T (CYLD-AS2)
NM_001042355.2:c.2792G>A (CYLD)	NP_001035814.1:p.Cys931Tyr
NM_001042412.2:c.2792G>A (CYLD)	NP_001035877.1:p.Cys931Tyr
NM_001042412.3:c.2792G>A (CYLD)	NP_001035877.1:p.Cys931Tyr
NM_001378743.1:c.2801G>A (CYLD) MANE Select	NP_001365672.1:p.Cys934Tyr
NM_001378744.1:c.2792G>A (CYLD)	NP_001365673.1:p.Cys931Tyr
NM_001378745.1:c.2792G>A (CYLD)	NP_001365674.1:p.Cys931Tyr
NM_001378746.1:c.2792G>A (CYLD)	NP_001365675.1:p.Cys931Tyr
NM_001378747.1:c.2792G>A (CYLD)	NP_001365676.1:p.Cys931Tyr
NM_001378748.1:c.2792G>A (CYLD)	NP_001365677.1:p.Cys931Tyr
NM_001378749.1:c.2792G>A (CYLD)	NP_001365678.1:p.Cys931Tyr
NM_001378750.1:c.2792G>A (CYLD)	NP_001365679.1:p.Cys931Tyr
NM_001378751.1:c.2762G>A (CYLD)	NP_001365680.1:p.Cys921Tyr
NM_001378752.1:c.2762G>A (CYLD)	NP_001365681.1:p.Cys921Tyr
NM_001378753.1:c.2762G>A (CYLD)	NP_001365682.1:p.Cys921Tyr
NM_001378754.1:c.2126G>A (CYLD)	NP_001365683.1:p.Cys709Tyr
NM_001378755.1:c.2126G>A (CYLD)	NP_001365684.1:p.Cys709Tyr
NM_015247.3:c.2801G>A (CYLD)	NP_056062.1:p.Cys934Tyr
NR_166071.1:n.2890G>A (CYLD)