Canonical Allele Identifier: CA733689759

Gene: WDR64

Linked Data

• dbSNP Id: rs1354245467
• MyVariant Identifiers: chr1:g.241960840_241960843del (hg19) ; chr1:g.241797538_241797541del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241797540_241797543del , CM000663.2:g.241797540_241797543del	GRCh38
NC_000001.10:g.241960842_241960845del , CM000663.1:g.241960842_241960845del	GRCh37
NC_000001.9:g.240027465_240027468del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425826.3:c.*1423+1170_*1423+1173del	ENSP00000406342.3:n.*1423+1170_*1423+1173del
ENST00000437684.7:c.3192+1170_3192+1173del MANE Select	ENSP00000402446.4:n.3192+1170_3192+1173del
ENST00000366552.6:c.3162+1170_3162+1173del	ENSP00000355510.2:n.3162+1170_3162+1173del
ENST00000414635.5:c.1974+1170_1974+1173del	ENSP00000406656.1:n.1974+1170_1974+1173del
ENST00000425826.2:c.1598+1170_1598+1173del
ENST00000437684.6:c.1825+1166_1825+1169del	ENSP00000402446.3:n.1825+1166_1825+1169del
NM_144625.4:c.3162+1170_3162+1173del	NP_653226.4:n.3162+1170_3162+1173del
XM_006711736.2:c.3192+1170_3192+1173del	XP_006711799.1:n.3192+1170_3192+1173del
XM_011544084.1:c.2709+1170_2709+1173del	XP_011542386.1:n.2709+1170_2709+1173del
XM_011544085.1:c.2709+1170_2709+1173del	XP_011542387.1:n.2709+1170_2709+1173del
XM_011544086.1:c.2709+1170_2709+1173del	XP_011542388.1:n.2709+1170_2709+1173del
XM_011544088.1:c.2253+1170_2253+1173del	XP_011542390.1:n.2253+1170_2253+1173del
XM_011544089.1:c.2199+1170_2199+1173del	XP_011542391.1:n.2199+1170_2199+1173del
XM_011544090.1:c.2199+1170_2199+1173del	XP_011542392.1:n.2199+1170_2199+1173del
XM_006711736.3:c.3192+1170_3192+1173del	XP_006711799.1:n.3192+1170_3192+1173del
XM_011544086.3:c.2709+1170_2709+1173del	XP_011542388.1:n.2709+1170_2709+1173del
XM_017000315.1:c.2940+1170_2940+1173del	XP_016855804.1:n.2940+1170_2940+1173del
NM_001367482.1:c.3192+1170_3192+1173del MANE Select	NP_001354411.1:n.3192+1170_3192+1173del