Canonical Allele Identifier: CA1229671674

Gene: WDR64

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241730933C= , CM000663.2:g.241730933C=	GRCh38
NC_000001.10:g.241894235C= , CM000663.1:g.241894235C=	GRCh37
NC_000001.9:g.239960858C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425826.3:c.1195-7430C=	ENSP00000406342.3:n.1195-7430C=
ENST00000437684.7:c.1195-7430C= MANE Select	ENSP00000402446.4:n.1195-7430C=
ENST00000366552.6:c.1165-7430C=	ENSP00000355510.2:n.1165-7430C=
ENST00000414635.5:c.478-7430C=	ENSP00000406656.1:n.478-7430C=
ENST00000437684.6:c.325-7430C=	ENSP00000402446.3:n.325-7430C=
NM_144625.4:c.1165-7430C=	NP_653226.4:n.1165-7430C=
XM_006711736.2:c.1195-7430C=	XP_006711799.1:n.1195-7430C=
XM_011544084.1:c.712-7430C=	XP_011542386.1:n.712-7430C=
XM_011544085.1:c.712-7430C=	XP_011542387.1:n.712-7430C=
XM_011544086.1:c.712-7430C=	XP_011542388.1:n.712-7430C=
XM_011544087.1:c.1195-7430C=	XP_011542389.1:n.1195-7430C=
XM_011544088.1:c.256-7430C=	XP_011542390.1:n.256-7430C=
XM_011544089.1:c.202-7430C=	XP_011542391.1:n.202-7430C=
XM_011544090.1:c.202-7430C=	XP_011542392.1:n.202-7430C=
XM_011544091.1:c.1195-7430C=	XP_011542393.1:n.1195-7430C=
XM_011544092.1:c.1195-7430C=	XP_011542394.1:n.1195-7430C=
XM_011544093.1:c.1195-7430C=	XP_011542395.1:n.1195-7430C=
XR_949326.1:n.54-2099G=
XM_006711736.3:c.1195-7430C=	XP_006711799.1:n.1195-7430C=
XM_011544086.3:c.712-7430C=	XP_011542388.1:n.712-7430C=
XM_011544087.2:c.1195-7430C=	XP_011542389.1:n.1195-7430C=
XM_011544092.2:c.1195-7430C=	XP_011542394.1:n.1195-7430C=
XM_017000315.1:c.943-7430C=	XP_016855804.1:n.943-7430C=
XR_002959419.1:n.1402-7430C=
NM_001367482.1:c.1195-7430C= MANE Select	NP_001354411.1:n.1195-7430C=