Canonical Allele Identifier: CA915945872
Gene: WAC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.28608427_28608430del , CM000672.2:g.28608427_28608430del GRCh38
NC_000010.10:g.28897356_28897359del , CM000672.1:g.28897356_28897359del GRCh37
NC_000010.9:g.28937362_28937365del NCBI36
NG_046603.1:g.80840_80843del

Transcript Alleles

HGVS Amino-acid Change
ENST00000495268.3:c.489_492del ENSP00000514964.1:p.Asn163LysfsTer7
ENST00000700325.1:c.1149_1152del ENSP00000514952.1:p.Asn383LysfsTer7
ENST00000706612.1:c.1149_1152del ENSP00000516469.1:p.Asn383LysfsTer7
ENST00000354911.9:c.1161_1164del MANE Select ENSP00000346986.4:p.Asn387LysfsTer7
ENST00000414108.6:c.1026_1029del ENSP00000415645.2:p.Asn342LysfsTer7
ENST00000420266.6:c.*1075_*1078del ENSP00000404758.2:n.*1075_*1078del
ENST00000428935.6:c.*170_*173del ENSP00000399706.3:n.*170_*173del
ENST00000442148.6:c.1026_1029del ENSP00000400848.2:p.Asn342LysfsTer7
ENST00000628285.3:c.*587_*590del ENSP00000486994.2:n.*587_*590del
ENST00000679398.1:c.1026_1029del ENSP00000506624.1:p.Asn342LysfsTer7
ENST00000679428.1:c.1026_1029del ENSP00000506445.1:p.Asn342LysfsTer7
ENST00000679570.1:c.*1156_*1159del ENSP00000506705.1:n.*1156_*1159del
ENST00000680735.1:c.1032_1035del ENSP00000505513.1:p.Asn344LysfsTer7
ENST00000681112.1:c.*1014_*1017del ENSP00000505444.1:n.*1014_*1017del
ENST00000345541.6:n.959_962del
ENST00000347934.8:c.852_855del ENSP00000311106.4:p.Asn284LysfsTer7
ENST00000354911.8:c.1161_1164del ENSP00000346986.4:p.Asn387LysfsTer7
ENST00000375646.5:c.717_720del ENSP00000364797.1:p.Asn239LysfsTer3
ENST00000375664.8:c.1026_1029del ENSP00000364816.3:p.Asn342LysfsTer7
ENST00000424454.5:c.*1169_*1172del ENSP00000404125.2:n.*1169_*1172del
ENST00000428935.5:c.*587_*590del ENSP00000399706.2:n.*587_*590del
ENST00000439676.5:c.1026_1029del ENSP00000415727.1:p.Asn342LysfsTer7
ENST00000476046.1:n.357_360del
ENST00000495268.2:n.82_85del
ENST00000628285.2:c.*587_*590del ENSP00000486994.1:n.*587_*590del
NM_016628.4:c.1161_1164del NP_057712.2:p.Asn387LysfsTer7
NM_100264.2:c.1026_1029del NP_567822.1:p.Asn342LysfsTer7
NM_100486.3:c.852_855del NP_567823.1:p.Asn284LysfsTer7
XM_005252454.2:c.1179_1182del XP_005252511.1:p.Asn393LysfsTer7
XM_011519491.1:c.1026_1029del XP_011517793.1:p.Asn342LysfsTer7
XR_930491.1:n.1081_1084del
XM_017016315.2:c.1026_1029del XP_016871804.1:p.Asn342LysfsTer7
XM_017016317.2:c.717_720del XP_016871806.1:p.Asn239LysfsTer7
XM_017016318.2:c.717_720del XP_016871807.1:p.Asn239LysfsTer7
XM_024448036.1:c.1026_1029del XP_024303804.1:p.Asn342LysfsTer7
XR_001747110.1:n.1116_1119del
XR_930491.2:n.1081_1084del
NM_016628.5:c.1161_1164del MANE Select NP_057712.2:p.Asn387LysfsTer7
NM_100264.3:c.1026_1029del NP_567822.1:p.Asn342LysfsTer7
NM_100486.4:c.852_855del NP_567823.1:p.Asn284LysfsTer7