Canonical Allele Identifier: CA733689783

Gene: WDR64

Linked Data

• dbSNP Id: rs1403080708
• MyVariant Identifiers: chr1:g.241960878_241960881del (hg19) ; chr1:g.241797576_241797579del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241797581_241797584del , CM000663.2:g.241797581_241797584del	GRCh38
NC_000001.10:g.241960883_241960886del , CM000663.1:g.241960883_241960886del	GRCh37
NC_000001.9:g.240027506_240027509del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425826.3:c.*1423+1211_*1423+1214del	ENSP00000406342.3:n.*1423+1211_*1423+1214del
ENST00000437684.7:c.3192+1211_3192+1214del MANE Select	ENSP00000402446.4:n.3192+1211_3192+1214del
ENST00000366552.6:c.3162+1211_3162+1214del	ENSP00000355510.2:n.3162+1211_3162+1214del
ENST00000414635.5:c.1974+1211_1974+1214del	ENSP00000406656.1:n.1974+1211_1974+1214del
ENST00000425826.2:c.1598+1211_1598+1214del
ENST00000437684.6:c.1825+1207_1825+1210del	ENSP00000402446.3:n.1825+1207_1825+1210del
NM_144625.4:c.3162+1211_3162+1214del	NP_653226.4:n.3162+1211_3162+1214del
XM_006711736.2:c.3192+1211_3192+1214del	XP_006711799.1:n.3192+1211_3192+1214del
XM_011544084.1:c.2709+1211_2709+1214del	XP_011542386.1:n.2709+1211_2709+1214del
XM_011544085.1:c.2709+1211_2709+1214del	XP_011542387.1:n.2709+1211_2709+1214del
XM_011544086.1:c.2709+1211_2709+1214del	XP_011542388.1:n.2709+1211_2709+1214del
XM_011544088.1:c.2253+1211_2253+1214del	XP_011542390.1:n.2253+1211_2253+1214del
XM_011544089.1:c.2199+1211_2199+1214del	XP_011542391.1:n.2199+1211_2199+1214del
XM_011544090.1:c.2199+1211_2199+1214del	XP_011542392.1:n.2199+1211_2199+1214del
XM_006711736.3:c.3192+1211_3192+1214del	XP_006711799.1:n.3192+1211_3192+1214del
XM_011544086.3:c.2709+1211_2709+1214del	XP_011542388.1:n.2709+1211_2709+1214del
XM_017000315.1:c.2940+1211_2940+1214del	XP_016855804.1:n.2940+1211_2940+1214del
NM_001367482.1:c.3192+1211_3192+1214del MANE Select	NP_001354411.1:n.3192+1211_3192+1214del