Canonical Allele Identifier: CA1229698600
Gene: WDR64 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241797325A= , CM000663.2:g.241797325A= GRCh38
NC_000001.10:g.241960627A= , CM000663.1:g.241960627A= GRCh37
NC_000001.9:g.240027250A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000425826.3:c.*1423+955A= ENSP00000406342.3:n.*1423+955A=
ENST00000437684.7:c.3192+955A= MANE Select ENSP00000402446.4:n.3192+955A=
ENST00000366552.6:c.3162+955A= ENSP00000355510.2:n.3162+955A=
ENST00000414635.5:c.1974+955A= ENSP00000406656.1:n.1974+955A=
ENST00000425826.2:c.1598+955A=
ENST00000437684.6:c.1825+951A= ENSP00000402446.3:n.1825+951A=
NM_144625.4:c.3162+955A= NP_653226.4:n.3162+955A=
XM_006711736.2:c.3192+955A= XP_006711799.1:n.3192+955A=
XM_011544084.1:c.2709+955A= XP_011542386.1:n.2709+955A=
XM_011544085.1:c.2709+955A= XP_011542387.1:n.2709+955A=
XM_011544086.1:c.2709+955A= XP_011542388.1:n.2709+955A=
XM_011544088.1:c.2253+955A= XP_011542390.1:n.2253+955A=
XM_011544089.1:c.2199+955A= XP_011542391.1:n.2199+955A=
XM_011544090.1:c.2199+955A= XP_011542392.1:n.2199+955A=
XM_006711736.3:c.3192+955A= XP_006711799.1:n.3192+955A=
XM_011544086.3:c.2709+955A= XP_011542388.1:n.2709+955A=
XM_017000315.1:c.2940+955A= XP_016855804.1:n.2940+955A=
NM_001367482.1:c.3192+955A= MANE Select NP_001354411.1:n.3192+955A=