Canonical Allele Identifier: CA395885640

Gene: CYLD CYLD-AS2

Linked Data

• MyVariant Identifiers: chr16:g.50830265T>C (hg19) ; chr16:g.50796354T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50796354T>C , CM000678.2:g.50796354T>C	GRCh38
NC_000016.9:g.50830265T>C , CM000678.1:g.50830265T>C	GRCh37
NC_000016.8:g.49387766T>C	NCBI36
NG_012061.1:g.59305T>C , LRG_491:g.59305T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427738.8:c.2717T>C (CYLD) MANE Select	ENSP00000392025.3:p.Val906Ala
ENST00000311559.13:c.2717T>C (CYLD)	ENSP00000308928.9:p.Val906Ala
ENST00000398568.6:c.2708T>C (CYLD)	ENSP00000381574.2:p.Val903Ala
ENST00000427738.7:c.2717T>C (CYLD)	ENSP00000392025.3:p.Val906Ala
ENST00000564326.5:c.2708T>C (CYLD)	ENSP00000454515.1:p.Val903Ala
ENST00000566024.1:c.177+1884T>C (CYLD)
ENST00000568704.2:c.2162T>C (CYLD)	ENSP00000456488.2:p.Val721Ala
ENST00000569418.5:c.2708T>C (CYLD)	ENSP00000457576.1:p.Val903Ala
NM_001042355.1:c.2708T>C (CYLD)	NP_001035814.1:p.Val903Ala
NM_001042412.1:c.2708T>C (CYLD)	NP_001035877.1:p.Val903Ala
NM_015247.2:c.2717T>C , LRG_491t1:c.2717T>C (CYLD)	NP_056062.1:p.Val906Ala
XM_005255812.2:c.2708T>C (CYLD)	XP_005255869.1:p.Val903Ala
XM_006721149.1:c.2708T>C (CYLD)	XP_006721212.1:p.Val903Ala
XM_011522906.1:c.2708T>C (CYLD)	XP_011521208.1:p.Val903Ala
XM_011522907.1:c.2708T>C (CYLD)	XP_011521209.1:p.Val903Ala
XM_011522908.1:c.2678T>C (CYLD)	XP_011521210.1:p.Val893Ala
XM_011522909.1:c.2677+1926T>C (CYLD)	XP_011521211.1:n.2677+1926T>C
XM_011522910.1:c.2677+1926T>C (CYLD)	XP_011521212.1:n.2677+1926T>C
XR_933218.1:n.3001T>C (CYLD)
XR_933542.1:n.2450+5769A>G (CYLD-AS2)
XM_011522907.2:c.2708T>C (CYLD)	XP_011521209.1:p.Val903Ala
XM_017022977.1:c.2708T>C (CYLD)	XP_016878466.1:p.Val903Ala
XM_017022978.1:c.2708T>C (CYLD)	XP_016878467.1:p.Val903Ala
XM_017022979.1:c.2708T>C (CYLD)	XP_016878468.1:p.Val903Ala
XM_017022980.1:c.2708T>C (CYLD)	XP_016878469.1:p.Val903Ala
XM_017022981.2:c.2678T>C (CYLD)	XP_016878470.1:p.Val893Ala
XR_001751849.1:n.2835T>C (CYLD)
XR_933542.2:n.4187+5769A>G (CYLD-AS2)
NM_001042355.2:c.2708T>C (CYLD)	NP_001035814.1:p.Val903Ala
NM_001042412.2:c.2708T>C (CYLD)	NP_001035877.1:p.Val903Ala
NM_001042412.3:c.2708T>C (CYLD)	NP_001035877.1:p.Val903Ala
NM_001378743.1:c.2717T>C (CYLD) MANE Select	NP_001365672.1:p.Val906Ala
NM_001378744.1:c.2708T>C (CYLD)	NP_001365673.1:p.Val903Ala
NM_001378745.1:c.2708T>C (CYLD)	NP_001365674.1:p.Val903Ala
NM_001378746.1:c.2708T>C (CYLD)	NP_001365675.1:p.Val903Ala
NM_001378747.1:c.2708T>C (CYLD)	NP_001365676.1:p.Val903Ala
NM_001378748.1:c.2708T>C (CYLD)	NP_001365677.1:p.Val903Ala
NM_001378749.1:c.2708T>C (CYLD)	NP_001365678.1:p.Val903Ala
NM_001378750.1:c.2708T>C (CYLD)	NP_001365679.1:p.Val903Ala
NM_001378751.1:c.2678T>C (CYLD)	NP_001365680.1:p.Val893Ala
NM_001378752.1:c.2678T>C (CYLD)	NP_001365681.1:p.Val893Ala
NM_001378753.1:c.2678T>C (CYLD)	NP_001365682.1:p.Val893Ala
NM_001378754.1:c.2042T>C (CYLD)	NP_001365683.1:p.Val681Ala
NM_001378755.1:c.2042T>C (CYLD)	NP_001365684.1:p.Val681Ala
NM_015247.3:c.2717T>C (CYLD)	NP_056062.1:p.Val906Ala
NR_166071.1:n.2806T>C (CYLD)