Canonical Allele Identifier: CA40355070
Gene: WDR64 HGNC NCBI

Linked Data

dbSNP Id: rs550652010

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241797559_241797561del , CM000663.2:g.241797559_241797561del GRCh38
NC_000001.10:g.241960861_241960863del , CM000663.1:g.241960861_241960863del GRCh37
NC_000001.9:g.240027484_240027486del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000425826.3:c.*1423+1189_*1423+1191del ENSP00000406342.3:n.*1423+1189_*1423+1191del
ENST00000437684.7:c.3192+1189_3192+1191del MANE Select ENSP00000402446.4:n.3192+1189_3192+1191del
ENST00000366552.6:c.3162+1189_3162+1191del ENSP00000355510.2:n.3162+1189_3162+1191del
ENST00000414635.5:c.1974+1189_1974+1191del ENSP00000406656.1:n.1974+1189_1974+1191del
ENST00000425826.2:c.1598+1189_1598+1191del
ENST00000437684.6:c.1825+1185_1825+1187del ENSP00000402446.3:n.1825+1185_1825+1187del
NM_144625.4:c.3162+1189_3162+1191del NP_653226.4:n.3162+1189_3162+1191del
XM_006711736.2:c.3192+1189_3192+1191del XP_006711799.1:n.3192+1189_3192+1191del
XM_011544084.1:c.2709+1189_2709+1191del XP_011542386.1:n.2709+1189_2709+1191del
XM_011544085.1:c.2709+1189_2709+1191del XP_011542387.1:n.2709+1189_2709+1191del
XM_011544086.1:c.2709+1189_2709+1191del XP_011542388.1:n.2709+1189_2709+1191del
XM_011544088.1:c.2253+1189_2253+1191del XP_011542390.1:n.2253+1189_2253+1191del
XM_011544089.1:c.2199+1189_2199+1191del XP_011542391.1:n.2199+1189_2199+1191del
XM_011544090.1:c.2199+1189_2199+1191del XP_011542392.1:n.2199+1189_2199+1191del
XM_006711736.3:c.3192+1189_3192+1191del XP_006711799.1:n.3192+1189_3192+1191del
XM_011544086.3:c.2709+1189_2709+1191del XP_011542388.1:n.2709+1189_2709+1191del
XM_017000315.1:c.2940+1189_2940+1191del XP_016855804.1:n.2940+1189_2940+1191del
NM_001367482.1:c.3192+1189_3192+1191del MANE Select NP_001354411.1:n.3192+1189_3192+1191del