Canonical Allele Identifier: CA281267984

Gene: CYLD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50781521C>T , CM000678.2:g.50781521C>T	GRCh38
NC_000016.9:g.50815432C>T , CM000678.1:g.50815432C>T	GRCh37
NC_000016.8:g.49372933C>T	NCBI36
NG_012061.1:g.44472C>T , LRG_491:g.44472C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378743.1:c.1684+110C>T MANE Select	NP_001365672.1:n.1684+110C>T
ENST00000427738.8:c.1684+110C>T MANE Select	ENSP00000392025.3:n.1684+110C>T
NM_001042355.1:c.1675+110C>T	NP_001035814.1:n.1675+110C>T
NM_001042355.2:c.1675+110C>T	NP_001035814.1:n.1675+110C>T
NM_001042412.1:c.1675+110C>T	NP_001035877.1:n.1675+110C>T
NM_001042412.2:c.1675+110C>T	NP_001035877.1:n.1675+110C>T
NM_001042412.3:c.1675+110C>T	NP_001035877.1:n.1675+110C>T
NM_001378744.1:c.1675+110C>T	NP_001365673.1:n.1675+110C>T
NM_001378745.1:c.1675+110C>T	NP_001365674.1:n.1675+110C>T
NM_001378746.1:c.1675+110C>T	NP_001365675.1:n.1675+110C>T
NM_001378747.1:c.1675+110C>T	NP_001365676.1:n.1675+110C>T
NM_001378748.1:c.1675+110C>T	NP_001365677.1:n.1675+110C>T
NM_001378749.1:c.1675+110C>T	NP_001365678.1:n.1675+110C>T
NM_001378750.1:c.1675+110C>T	NP_001365679.1:n.1675+110C>T
NM_001378751.1:c.1645+110C>T	NP_001365680.1:n.1645+110C>T
NM_001378752.1:c.1645+110C>T	NP_001365681.1:n.1645+110C>T
NM_001378753.1:c.1645+110C>T	NP_001365682.1:n.1645+110C>T
NM_001378754.1:c.1009+110C>T	NP_001365683.1:n.1009+110C>T
NM_001378755.1:c.1009+110C>T	NP_001365684.1:n.1009+110C>T
NM_015247.2:c.1684+110C>T , LRG_491t1:c.1684+110C>T	NP_056062.1:n.1684+110C>T
NM_015247.3:c.1684+110C>T	NP_056062.1:n.1684+110C>T
NR_166071.1:n.1774-804C>T
ENST00000311559.13:c.1684+110C>T	ENSP00000308928.9:n.1684+110C>T
ENST00000398568.6:c.1675+110C>T	ENSP00000381574.2:n.1675+110C>T
ENST00000427738.7:c.1684+110C>T	ENSP00000392025.3:n.1684+110C>T
ENST00000563629.1:n.1411+110C>T
ENST00000564326.5:c.1675+110C>T	ENSP00000454515.1:n.1675+110C>T
ENST00000566206.5:c.1675+110C>T	ENSP00000462134.1:n.1675+110C>T
ENST00000568704.2:c.1130-804C>T	ENSP00000456488.2:n.1130-804C>T
ENST00000569418.5:c.1675+110C>T	ENSP00000457576.1:n.1675+110C>T
ENST00000569891.5:n.2070+110C>T
XM_005255812.2:c.1675+110C>T	XP_005255869.1:n.1675+110C>T
XM_006721149.1:c.1675+110C>T	XP_006721212.1:n.1675+110C>T
XM_011522906.1:c.1675+110C>T	XP_011521208.1:n.1675+110C>T
XM_011522907.1:c.1675+110C>T	XP_011521209.1:n.1675+110C>T
XM_011522907.2:c.1675+110C>T	XP_011521209.1:n.1675+110C>T
XM_011522908.1:c.1645+110C>T	XP_011521210.1:n.1645+110C>T
XM_011522909.1:c.1675+110C>T	XP_011521211.1:n.1675+110C>T
XM_011522910.1:c.1675+110C>T	XP_011521212.1:n.1675+110C>T
XM_011522911.1:c.1675+110C>T	XP_011521213.1:n.1675+110C>T
XM_011522911.2:c.1675+110C>T	XP_011521213.1:n.1675+110C>T
XM_017022977.1:c.1675+110C>T	XP_016878466.1:n.1675+110C>T
XM_017022978.1:c.1675+110C>T	XP_016878467.1:n.1675+110C>T
XM_017022979.1:c.1675+110C>T	XP_016878468.1:n.1675+110C>T
XM_017022980.1:c.1675+110C>T	XP_016878469.1:n.1675+110C>T
XM_017022981.2:c.1645+110C>T	XP_016878470.1:n.1645+110C>T
XR_001751849.1:n.1803-804C>T
XR_933218.1:n.1968+110C>T