Canonical Allele Identifier: CA14363846
Gene: CYLD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50747891T>C , CM000678.2:g.50747891T>C GRCh38
NC_000016.9:g.50781802T>C , CM000678.1:g.50781802T>C GRCh37
NC_000016.8:g.49339303T>C NCBI36
NG_012061.1:g.10842T>C , LRG_491:g.10842T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000427738.8:c.-123-1685T>C MANE Select ENSP00000392025.3:n.-123-1685T>C
ENST00000311559.13:c.-123-1685T>C ENSP00000308928.9:n.-123-1685T>C
ENST00000398568.6:c.-123-1685T>C ENSP00000381574.2:n.-123-1685T>C
ENST00000427738.7:c.-123-1685T>C ENSP00000392025.3:n.-123-1685T>C
ENST00000564326.5:c.-150-1658T>C ENSP00000454515.1:n.-150-1658T>C
ENST00000564634.5:c.-123-1685T>C ENSP00000455535.1:n.-123-1685T>C
ENST00000566206.5:c.-150-1658T>C ENSP00000462134.1:n.-150-1658T>C
ENST00000566679.6:c.-150-1658T>C ENSP00000456912.2:n.-150-1658T>C
ENST00000569418.5:c.-123-1685T>C ENSP00000457576.1:n.-123-1685T>C
ENST00000569681.5:c.-123-1685T>C ENSP00000457108.1:n.-123-1685T>C
ENST00000569891.5:n.273-1685T>C
NM_001042355.1:c.-123-1685T>C NP_001035814.1:n.-123-1685T>C
NM_001042412.1:c.-123-1685T>C NP_001035877.1:n.-123-1685T>C
NM_015247.2:c.-123-1685T>C , LRG_491t1:c.-123-1685T>C NP_056062.1:n.-123-1685T>C
XM_005255812.2:c.-123-1685T>C XP_005255869.1:n.-123-1685T>C
XM_006721149.1:c.-123-1685T>C XP_006721212.1:n.-123-1685T>C
XM_011522906.1:c.-150-1658T>C XP_011521208.1:n.-150-1658T>C
XM_011522907.1:c.-50-1758T>C XP_011521209.1:n.-50-1758T>C
XM_011522908.1:c.-123-1685T>C XP_011521210.1:n.-123-1685T>C
XM_011522909.1:c.-123-1685T>C XP_011521211.1:n.-123-1685T>C
XM_011522910.1:c.-123-1685T>C XP_011521212.1:n.-123-1685T>C
XM_011522911.1:c.-123-1685T>C XP_011521213.1:n.-123-1685T>C
XR_933218.1:n.171-1685T>C
XM_011522907.2:c.-50-1758T>C XP_011521209.1:n.-50-1758T>C
XM_011522911.2:c.-123-1685T>C XP_011521213.1:n.-123-1685T>C
XM_017022977.1:c.-123-1685T>C XP_016878466.1:n.-123-1685T>C
XM_017022978.1:c.-150-1658T>C XP_016878467.1:n.-150-1658T>C
XM_017022979.1:c.-150-1658T>C XP_016878468.1:n.-150-1658T>C
XM_017022980.1:c.-50-1758T>C XP_016878469.1:n.-50-1758T>C
XM_017022981.2:c.-123-1685T>C XP_016878470.1:n.-123-1685T>C
XR_001751849.1:n.171-1685T>C
NM_001042355.2:c.-123-1685T>C NP_001035814.1:n.-123-1685T>C
NM_001042412.2:c.-123-1685T>C NP_001035877.1:n.-123-1685T>C
NM_001042412.3:c.-123-1685T>C NP_001035877.1:n.-123-1685T>C
NM_001378743.1:c.-123-1685T>C MANE Select NP_001365672.1:n.-123-1685T>C
NM_001378744.1:c.-150-1658T>C NP_001365673.1:n.-150-1658T>C
NM_001378745.1:c.-123-1685T>C NP_001365674.1:n.-123-1685T>C
NM_001378746.1:c.-123-1685T>C NP_001365675.1:n.-123-1685T>C
NM_001378747.1:c.-50-1758T>C NP_001365676.1:n.-50-1758T>C
NM_001378748.1:c.-123-1685T>C NP_001365677.1:n.-123-1685T>C
NM_001378749.1:c.-50-1758T>C NP_001365678.1:n.-50-1758T>C
NM_001378750.1:c.-123-1685T>C NP_001365679.1:n.-123-1685T>C
NM_001378751.1:c.-123-1685T>C NP_001365680.1:n.-123-1685T>C
NM_001378752.1:c.-123-1685T>C NP_001365681.1:n.-123-1685T>C
NM_001378753.1:c.-150-1658T>C NP_001365682.1:n.-150-1658T>C
NM_001378754.1:c.-785-1685T>C NP_001365683.1:n.-785-1685T>C
NM_001378755.1:c.-785-1685T>C NP_001365684.1:n.-785-1685T>C
NM_015247.3:c.-123-1685T>C NP_056062.1:n.-123-1685T>C
NR_166071.1:n.142-1685T>C
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