Canonical Allele Identifier: CA733689770

Gene: WDR64

Linked Data

• dbSNP Id: rs1318171472
• gnomAD v3: 1-241797559-CAAT-C
• gnomAD v4: 1-241797559-CAAT-C
• MyVariant Identifiers: chr1:g.241960862_241960864del (hg19) ; chr1:g.241797560_241797562del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241797561_241797563del , CM000663.2:g.241797561_241797563del	GRCh38
NC_000001.10:g.241960863_241960865del , CM000663.1:g.241960863_241960865del	GRCh37
NC_000001.9:g.240027486_240027488del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425826.3:c.*1423+1191_*1423+1193del	ENSP00000406342.3:n.*1423+1191_*1423+1193del
ENST00000437684.7:c.3192+1191_3192+1193del MANE Select	ENSP00000402446.4:n.3192+1191_3192+1193del
ENST00000366552.6:c.3162+1191_3162+1193del	ENSP00000355510.2:n.3162+1191_3162+1193del
ENST00000414635.5:c.1974+1191_1974+1193del	ENSP00000406656.1:n.1974+1191_1974+1193del
ENST00000425826.2:c.1598+1191_1598+1193del
ENST00000437684.6:c.1825+1187_1825+1189del	ENSP00000402446.3:n.1825+1187_1825+1189del
NM_144625.4:c.3162+1191_3162+1193del	NP_653226.4:n.3162+1191_3162+1193del
XM_006711736.2:c.3192+1191_3192+1193del	XP_006711799.1:n.3192+1191_3192+1193del
XM_011544084.1:c.2709+1191_2709+1193del	XP_011542386.1:n.2709+1191_2709+1193del
XM_011544085.1:c.2709+1191_2709+1193del	XP_011542387.1:n.2709+1191_2709+1193del
XM_011544086.1:c.2709+1191_2709+1193del	XP_011542388.1:n.2709+1191_2709+1193del
XM_011544088.1:c.2253+1191_2253+1193del	XP_011542390.1:n.2253+1191_2253+1193del
XM_011544089.1:c.2199+1191_2199+1193del	XP_011542391.1:n.2199+1191_2199+1193del
XM_011544090.1:c.2199+1191_2199+1193del	XP_011542392.1:n.2199+1191_2199+1193del
XM_006711736.3:c.3192+1191_3192+1193del	XP_006711799.1:n.3192+1191_3192+1193del
XM_011544086.3:c.2709+1191_2709+1193del	XP_011542388.1:n.2709+1191_2709+1193del
XM_017000315.1:c.2940+1191_2940+1193del	XP_016855804.1:n.2940+1191_2940+1193del
NM_001367482.1:c.3192+1191_3192+1193del MANE Select	NP_001354411.1:n.3192+1191_3192+1193del