Canonical Allele Identifier: CA1229671642
Gene: WDR64 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241730858_241730864delinsATCAAGT , CM000663.2:g.241730858_241730864delinsATCAAGT GRCh38
NC_000001.10:g.241894160_241894166delinsATCAAGT , CM000663.1:g.241894160_241894166delinsATCAAGT GRCh37
NC_000001.9:g.239960783_239960789delinsATCAAGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000425826.3:c.1194+7422_1194+7428delinsATCAAGT ENSP00000406342.3:n.1194+7422_1194+7428de...
ENST00000437684.7:c.1194+7422_1194+7428delinsATCAAGT MANE Select ENSP00000402446.4:n.1194+7422_1194+7428de...
ENST00000366552.6:c.1164+7422_1164+7428delinsATCAAGT ENSP00000355510.2:n.1164+7422_1164+7428de...
ENST00000414635.5:c.477+7422_477+7428delinsATCAAGT ENSP00000406656.1:n.477+7422_477+7428deli...
ENST00000437684.6:c.324+7422_324+7428delinsATCAAGT ENSP00000402446.3:n.324+7422_324+7428deli...
NM_144625.4:c.1164+7422_1164+7428delinsATCAAGT NP_653226.4:n.1164+7422_1164+7428delinsAT...
XM_006711736.2:c.1194+7422_1194+7428delinsATCAAGT XP_006711799.1:n.1194+7422_1194+7428delin...
XM_011544084.1:c.711+7422_711+7428delinsATCAAGT XP_011542386.1:n.711+7422_711+7428delinsA...
XM_011544085.1:c.711+7422_711+7428delinsATCAAGT XP_011542387.1:n.711+7422_711+7428delinsA...
XM_011544086.1:c.711+7422_711+7428delinsATCAAGT XP_011542388.1:n.711+7422_711+7428delinsA...
XM_011544087.1:c.1194+7422_1194+7428delinsATCAAGT XP_011542389.1:n.1194+7422_1194+7428delin...
XM_011544088.1:c.255+7422_255+7428delinsATCAAGT XP_011542390.1:n.255+7422_255+7428delinsA...
XM_011544089.1:c.201+7422_201+7428delinsATCAAGT XP_011542391.1:n.201+7422_201+7428delinsA...
XM_011544090.1:c.201+7422_201+7428delinsATCAAGT XP_011542392.1:n.201+7422_201+7428delinsA...
XM_011544091.1:c.1194+7422_1194+7428delinsATCAAGT XP_011542393.1:n.1194+7422_1194+7428delin...
XM_011544092.1:c.1194+7422_1194+7428delinsATCAAGT XP_011542394.1:n.1194+7422_1194+7428delin...
XM_011544093.1:c.1194+7422_1194+7428delinsATCAAGT XP_011542395.1:n.1194+7422_1194+7428delin...
XR_949326.1:n.54-2030_54-2024delinsACTTGAT
XM_006711736.3:c.1194+7422_1194+7428delinsATCAAGT XP_006711799.1:n.1194+7422_1194+7428delin...
XM_011544086.3:c.711+7422_711+7428delinsATCAAGT XP_011542388.1:n.711+7422_711+7428delinsA...
XM_011544087.2:c.1194+7422_1194+7428delinsATCAAGT XP_011542389.1:n.1194+7422_1194+7428delin...
XM_011544092.2:c.1194+7422_1194+7428delinsATCAAGT XP_011542394.1:n.1194+7422_1194+7428delin...
XM_017000315.1:c.942+7422_942+7428delinsATCAAGT XP_016855804.1:n.942+7422_942+7428delinsA...
XR_002959419.1:n.1401+7422_1401+7428delinsATCAAGT
NM_001367482.1:c.1194+7422_1194+7428delinsATCAAGT MANE Select NP_001354411.1:n.1194+7422_1194+7428delin...