Canonical Allele Identifier: CA1229698618

Gene: WDR64

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241797374G= , CM000663.2:g.241797374G=	GRCh38
NC_000001.10:g.241960676G= , CM000663.1:g.241960676G=	GRCh37
NC_000001.9:g.240027299G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000425826.3:c.*1423+1004G=	ENSP00000406342.3:n.*1423+1004G=
ENST00000437684.7:c.3192+1004G= MANE Select	ENSP00000402446.4:n.3192+1004G=
ENST00000366552.6:c.3162+1004G=	ENSP00000355510.2:n.3162+1004G=
ENST00000414635.5:c.1974+1004G=	ENSP00000406656.1:n.1974+1004G=
ENST00000425826.2:c.1598+1004G=
ENST00000437684.6:c.1825+1000G=	ENSP00000402446.3:n.1825+1000G=
NM_144625.4:c.3162+1004G=	NP_653226.4:n.3162+1004G=
XM_006711736.2:c.3192+1004G=	XP_006711799.1:n.3192+1004G=
XM_011544084.1:c.2709+1004G=	XP_011542386.1:n.2709+1004G=
XM_011544085.1:c.2709+1004G=	XP_011542387.1:n.2709+1004G=
XM_011544086.1:c.2709+1004G=	XP_011542388.1:n.2709+1004G=
XM_011544088.1:c.2253+1004G=	XP_011542390.1:n.2253+1004G=
XM_011544089.1:c.2199+1004G=	XP_011542391.1:n.2199+1004G=
XM_011544090.1:c.2199+1004G=	XP_011542392.1:n.2199+1004G=
XM_006711736.3:c.3192+1004G=	XP_006711799.1:n.3192+1004G=
XM_011544086.3:c.2709+1004G=	XP_011542388.1:n.2709+1004G=
XM_017000315.1:c.2940+1004G=	XP_016855804.1:n.2940+1004G=
NM_001367482.1:c.3192+1004G= MANE Select	NP_001354411.1:n.3192+1004G=