Canonical Allele Identifier: CA395882698

Gene: CYLD CYLD-AS2

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50794429G>A , CM000678.2:g.50794429G>A	GRCh38
NC_000016.9:g.50828340G>A , CM000678.1:g.50828340G>A	GRCh37
NC_000016.8:g.49385841G>A	NCBI36
NG_012061.1:g.57380G>A , LRG_491:g.57380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427738.8:c.2686+1G>A (CYLD) MANE Select	ENSP00000392025.3:n.2686+1G>A
ENST00000311559.13:c.2686+1G>A (CYLD)	ENSP00000308928.9:n.2686+1G>A
ENST00000398568.6:c.2677+1G>A (CYLD)	ENSP00000381574.2:n.2677+1G>A
ENST00000427738.7:c.2686+1G>A (CYLD)	ENSP00000392025.3:n.2686+1G>A
ENST00000562884.1:c.266G>A (CYLD)	ENSP00000463197.1:p.Gly89Asp
ENST00000564326.5:c.2677+1G>A (CYLD)	ENSP00000454515.1:n.2677+1G>A
ENST00000566024.1:c.136G>A (CYLD)
ENST00000566206.5:c.2677+1G>A (CYLD)	ENSP00000462134.1:n.2677+1G>A
ENST00000568704.2:c.2131+1G>A (CYLD)	ENSP00000456488.2:n.2131+1G>A
ENST00000569418.5:c.2677+1G>A (CYLD)	ENSP00000457576.1:n.2677+1G>A
NM_001042355.1:c.2677+1G>A (CYLD)	NP_001035814.1:n.2677+1G>A
NM_001042412.1:c.2677+1G>A (CYLD)	NP_001035877.1:n.2677+1G>A
NM_015247.2:c.2686+1G>A , LRG_491t1:c.2686+1G>A (CYLD)	NP_056062.1:n.2686+1G>A
XM_005255812.2:c.2677+1G>A (CYLD)	XP_005255869.1:n.2677+1G>A
XM_006721149.1:c.2677+1G>A (CYLD)	XP_006721212.1:n.2677+1G>A
XM_011522906.1:c.2677+1G>A (CYLD)	XP_011521208.1:n.2677+1G>A
XM_011522907.1:c.2677+1G>A (CYLD)	XP_011521209.1:n.2677+1G>A
XM_011522908.1:c.2647+1G>A (CYLD)	XP_011521210.1:n.2647+1G>A
XM_011522909.1:c.2677+1G>A (CYLD)	XP_011521211.1:n.2677+1G>A
XM_011522910.1:c.2677+1G>A (CYLD)	XP_011521212.1:n.2677+1G>A
XR_933218.1:n.2970+1G>A (CYLD)
XR_933542.1:n.2450+7694C>T (CYLD-AS2)
XM_011522907.2:c.2677+1G>A (CYLD)	XP_011521209.1:n.2677+1G>A
XM_017022977.1:c.2677+1G>A (CYLD)	XP_016878466.1:n.2677+1G>A
XM_017022978.1:c.2677+1G>A (CYLD)	XP_016878467.1:n.2677+1G>A
XM_017022979.1:c.2677+1G>A (CYLD)	XP_016878468.1:n.2677+1G>A
XM_017022980.1:c.2677+1G>A (CYLD)	XP_016878469.1:n.2677+1G>A
XM_017022981.2:c.2647+1G>A (CYLD)	XP_016878470.1:n.2647+1G>A
XR_001751849.1:n.2804+1G>A (CYLD)
XR_933542.2:n.4187+7694C>T (CYLD-AS2)
NM_001042355.2:c.2677+1G>A (CYLD)	NP_001035814.1:n.2677+1G>A
NM_001042412.2:c.2677+1G>A (CYLD)	NP_001035877.1:n.2677+1G>A
NM_001042412.3:c.2677+1G>A (CYLD)	NP_001035877.1:n.2677+1G>A
NM_001378743.1:c.2686+1G>A (CYLD) MANE Select	NP_001365672.1:n.2686+1G>A
NM_001378744.1:c.2677+1G>A (CYLD)	NP_001365673.1:n.2677+1G>A
NM_001378745.1:c.2677+1G>A (CYLD)	NP_001365674.1:n.2677+1G>A
NM_001378746.1:c.2677+1G>A (CYLD)	NP_001365675.1:n.2677+1G>A
NM_001378747.1:c.2677+1G>A (CYLD)	NP_001365676.1:n.2677+1G>A
NM_001378748.1:c.2677+1G>A (CYLD)	NP_001365677.1:n.2677+1G>A
NM_001378749.1:c.2677+1G>A (CYLD)	NP_001365678.1:n.2677+1G>A
NM_001378750.1:c.2677+1G>A (CYLD)	NP_001365679.1:n.2677+1G>A
NM_001378751.1:c.2647+1G>A (CYLD)	NP_001365680.1:n.2647+1G>A
NM_001378752.1:c.2647+1G>A (CYLD)	NP_001365681.1:n.2647+1G>A
NM_001378753.1:c.2647+1G>A (CYLD)	NP_001365682.1:n.2647+1G>A
NM_001378754.1:c.2011+1G>A (CYLD)	NP_001365683.1:n.2011+1G>A
NM_001378755.1:c.2011+1G>A (CYLD)	NP_001365684.1:n.2011+1G>A
NM_015247.3:c.2686+1G>A (CYLD)	NP_056062.1:n.2686+1G>A
NR_166071.1:n.2775+1G>A (CYLD)