Canonical Allele Identifier: CA1014060203

Gene: WDR64

Linked Data

• dbSNP Id: rs1669052067
• gnomAD v3: 1-241730907-T-C
• gnomAD v4: 1-241730907-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241730907T>C , CM000663.2:g.241730907T>C	GRCh38
NC_000001.10:g.241894209T>C , CM000663.1:g.241894209T>C	GRCh37
NC_000001.9:g.239960832T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425826.3:c.1195-7456T>C	ENSP00000406342.3:n.1195-7456T>C
ENST00000437684.7:c.1195-7456T>C MANE Select	ENSP00000402446.4:n.1195-7456T>C
ENST00000366552.6:c.1165-7456T>C	ENSP00000355510.2:n.1165-7456T>C
ENST00000414635.5:c.478-7456T>C	ENSP00000406656.1:n.478-7456T>C
ENST00000437684.6:c.325-7456T>C	ENSP00000402446.3:n.325-7456T>C
NM_144625.4:c.1165-7456T>C	NP_653226.4:n.1165-7456T>C
XM_006711736.2:c.1195-7456T>C	XP_006711799.1:n.1195-7456T>C
XM_011544084.1:c.712-7456T>C	XP_011542386.1:n.712-7456T>C
XM_011544085.1:c.712-7456T>C	XP_011542387.1:n.712-7456T>C
XM_011544086.1:c.712-7456T>C	XP_011542388.1:n.712-7456T>C
XM_011544087.1:c.1195-7456T>C	XP_011542389.1:n.1195-7456T>C
XM_011544088.1:c.256-7456T>C	XP_011542390.1:n.256-7456T>C
XM_011544089.1:c.202-7456T>C	XP_011542391.1:n.202-7456T>C
XM_011544090.1:c.202-7456T>C	XP_011542392.1:n.202-7456T>C
XM_011544091.1:c.1195-7456T>C	XP_011542393.1:n.1195-7456T>C
XM_011544092.1:c.1195-7456T>C	XP_011542394.1:n.1195-7456T>C
XM_011544093.1:c.1195-7456T>C	XP_011542395.1:n.1195-7456T>C
XR_949326.1:n.54-2073A>G
XM_006711736.3:c.1195-7456T>C	XP_006711799.1:n.1195-7456T>C
XM_011544086.3:c.712-7456T>C	XP_011542388.1:n.712-7456T>C
XM_011544087.2:c.1195-7456T>C	XP_011542389.1:n.1195-7456T>C
XM_011544092.2:c.1195-7456T>C	XP_011542394.1:n.1195-7456T>C
XM_017000315.1:c.943-7456T>C	XP_016855804.1:n.943-7456T>C
XR_002959419.1:n.1402-7456T>C
NM_001367482.1:c.1195-7456T>C MANE Select	NP_001354411.1:n.1195-7456T>C