Canonical Allele Identifier: CA281292618

Gene: CYLD CYLD-AS1

Linked Data

• dbSNP Id: rs1020043545
• gnomAD v2: 16-50776005-G-T
• gnomAD v3: 16-50742094-G-T
• gnomAD v4: 16-50742094-G-T
• MyVariant Identifiers: chr16:g.50776005G>T (hg19) ; chr16:g.50742094G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50742094G>T , CM000678.2:g.50742094G>T	GRCh38
NC_000016.9:g.50776005G>T , CM000678.1:g.50776005G>T	GRCh37
NC_000016.8:g.49333506G>T	NCBI36
NG_012061.1:g.5045G>T , LRG_491:g.5045G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427738.8:c.-234G>T (CYLD) MANE Select	ENSP00000392025.3:n.-234G>T
ENST00000311559.13:c.-371G>T (CYLD)	ENSP00000308928.9:n.-371G>T
ENST00000564326.5:c.-181G>T (CYLD)	ENSP00000454515.1:n.-181G>T
ENST00000566206.5:c.-242G>T (CYLD)	ENSP00000462134.1:n.-242G>T
ENST00000569418.5:c.-234G>T (CYLD)	ENSP00000457576.1:n.-234G>T
ENST00000569681.5:c.-234G>T (CYLD)	ENSP00000457108.1:n.-234G>T
ENST00000569891.5:n.25G>T (CYLD)
NM_001042355.1:c.-234G>T (CYLD)	NP_001035814.1:n.-234G>T
NM_015247.2:c.-371G>T , LRG_491t1:c.-371G>T (CYLD)	NP_056062.1:n.-371G>T
XM_005255812.2:c.-371G>T (CYLD)	XP_005255869.1:n.-371G>T
XR_933543.1:n.62+577C>A (CYLD-AS1)
XR_933544.1:n.85+577C>A (CYLD-AS1)
XR_933545.1:n.85+577C>A (CYLD-AS1)
XR_933546.1:n.85+577C>A (CYLD-AS1)
XR_933547.1:n.145+577C>A (CYLD-AS1)
XR_933548.1:n.145+577C>A (CYLD-AS1)
XM_017022979.1:c.-261G>T (CYLD)	XP_016878468.1:n.-261G>T
XM_017022981.2:c.-234G>T (CYLD)	XP_016878470.1:n.-234G>T
XR_001752046.2:n.199+577C>A (CYLD-AS1)
NM_001042355.2:c.-234G>T (CYLD)	NP_001035814.1:n.-234G>T
NM_001042412.2:c.-326G>T (CYLD)	NP_001035877.1:n.-326G>T
NM_001378743.1:c.-234G>T (CYLD) MANE Select	NP_001365672.1:n.-234G>T
NM_001378744.1:c.-261G>T (CYLD)	NP_001365673.1:n.-261G>T
NM_001378745.1:c.-371G>T (CYLD)	NP_001365674.1:n.-371G>T
NM_001378749.1:c.-161G>T (CYLD)	NP_001365678.1:n.-161G>T
NM_001378751.1:c.-234G>T (CYLD)	NP_001365680.1:n.-234G>T
NM_001378753.1:c.-261G>T (CYLD)	NP_001365682.1:n.-261G>T
NM_001378754.1:c.-896G>T (CYLD)	NP_001365683.1:n.-896G>T
NM_015247.3:c.-371G>T (CYLD)	NP_056062.1:n.-371G>T