Canonical Allele Identifier: CA1140066760

Gene: WDR64

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241750006T= , CM000663.2:g.241750006T=	GRCh38
NC_000001.10:g.241913308T= , CM000663.1:g.241913308T=	GRCh37
NC_000001.9:g.239979931T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425826.3:c.1771-154T=	ENSP00000406342.3:n.1771-154T=
ENST00000437684.7:c.1770+284T= MANE Select	ENSP00000402446.4:n.1770+284T=
ENST00000366552.6:c.1740+284T=	ENSP00000355510.2:n.1740+284T=
ENST00000414635.5:c.1053+284T=	ENSP00000406656.1:n.1053+284T=
ENST00000425826.2:c.176+284T=
ENST00000437684.6:c.900+284T=	ENSP00000402446.3:n.900+284T=
ENST00000472717.6:c.417+284T=	ENSP00000431729.2:n.417+284T=
NM_144625.4:c.1740+284T=	NP_653226.4:n.1740+284T=
XM_006711736.2:c.1770+284T=	XP_006711799.1:n.1770+284T=
XM_011544084.1:c.1287+284T=	XP_011542386.1:n.1287+284T=
XM_011544085.1:c.1287+284T=	XP_011542387.1:n.1287+284T=
XM_011544086.1:c.1287+284T=	XP_011542388.1:n.1287+284T=
XM_011544087.1:c.1770+284T=	XP_011542389.1:n.1770+284T=
XM_011544088.1:c.831+284T=	XP_011542390.1:n.831+284T=
XM_011544089.1:c.777+284T=	XP_011542391.1:n.777+284T=
XM_011544090.1:c.777+284T=	XP_011542392.1:n.777+284T=
XM_011544091.1:c.1770+284T=	XP_011542393.1:n.1770+284T=
XM_011544092.1:c.1770+284T=	XP_011542394.1:n.1770+284T=
XM_011544093.1:c.1770+284T=	XP_011542395.1:n.1770+284T=
XM_006711736.3:c.1770+284T=	XP_006711799.1:n.1770+284T=
XM_011544086.3:c.1287+284T=	XP_011542388.1:n.1287+284T=
XM_011544087.2:c.1770+284T=	XP_011542389.1:n.1770+284T=
XM_011544092.2:c.1770+284T=	XP_011542394.1:n.1770+284T=
XM_017000315.1:c.1518+284T=	XP_016855804.1:n.1518+284T=
XR_002959419.1:n.1978-154T=
NM_001367482.1:c.1770+284T= MANE Select	NP_001354411.1:n.1770+284T=