Canonical Allele Identifier: CA344722552

Gene: WDR26

Linked Data

• ClinVar Variation Id: 522069
• ClinVar RCV Id: RCV000623249
• dbSNP Id: rs1553350638
• gnomAD v3: 1-224389854-C-A
• gnomAD v4: 1-224389854-C-A
• MyVariant Identifiers: chr1:g.224577556C>A (hg19) ; chr1:g.224389854C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.224389854C>A , CM000663.2:g.224389854C>A	GRCh38
NC_000001.10:g.224577556C>A , CM000663.1:g.224577556C>A	GRCh37
NC_000001.9:g.222644179C>A	NCBI36
NG_047198.1:g.49446G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443112.7:n.3757G>T
ENST00000704632.1:c.1633G>T	ENSP00000515968.1:n.1633G>T
ENST00000704640.1:c.1463G>T
ENST00000414423.9:c.2267G>T MANE Select	ENSP00000408108.4:p.Cys756Phe
ENST00000651911.2:c.1809G>T
ENST00000678555.1:c.2081G>T	ENSP00000504302.1:p.Cys694Phe
ENST00000678879.1:c.1732G>T
ENST00000678917.1:c.1967G>T	ENSP00000504428.1:p.Cys656Phe
ENST00000414423.6:c.1967G>T	ENSP00000408108.2:p.Cys656Phe
ENST00000480676.2:c.867G>T
ENST00000486652.5:c.2149G>T	ENSP00000422758.1:n.2149G>T
NM_001115113.2:c.1919G>T	NP_001108585.2:p.Cys640Phe
NM_025160.6:c.1967G>T	NP_079436.4:p.Cys656Phe
XM_005273273.3:c.1781G>T	XP_005273330.1:p.Cys594Phe
XM_006711817.2:c.1964G>T	XP_006711880.1:p.Cys655Phe
XM_011544281.1:c.1337G>T	XP_011542583.1:p.Cys446Phe
XM_011544282.1:c.1196G>T	XP_011542584.1:p.Cys399Phe
XM_005273273.5:c.1781G>T	XP_005273330.1:p.Cys594Phe
XM_006711817.4:c.1964G>T	XP_006711880.1:p.Cys655Phe
XM_011544281.2:c.1337G>T	XP_011542583.1:p.Cys446Phe
XM_011544282.2:c.1196G>T	XP_011542584.1:p.Cys399Phe
XM_017002396.1:c.1337G>T	XP_016857885.1:p.Cys446Phe
XR_001737437.2:n.2431G>T
XR_002957642.1:n.4095G>T
XR_002957643.1:n.3909G>T
XR_002957644.1:n.4165G>T
NM_001115113.3:c.1919G>T	NP_001108585.2:p.Cys640Phe
NM_001379403.1:c.2267G>T MANE Select	NP_001366332.1:p.Cys756Phe
NM_025160.7:c.1967G>T	NP_079436.4:p.Cys656Phe