Canonical Allele Identifier: CA658683172

Gene: WDR26

Linked Data

• ClinVar Variation Id: 488458
• ClinVar RCV Id: RCV000578316
• dbSNP Id: rs1553364018
• MyVariant Identifiers: chr1:g.224621734_224621735insT (hg19) ; chr1:g.224434032_224434033insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.224434032_224434033insT , CM000663.2:g.224434032_224434033insT	GRCh38
NC_000001.10:g.224621734_224621735insT , CM000663.1:g.224621734_224621735insT	GRCh37
NC_000001.9:g.222688357_222688358insT	NCBI36
NG_047198.1:g.5267_5268insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000414423.9:c.373_374insA MANE Select	ENSP00000408108.4:p.Gly125GlufsTer?
ENST00000678307.1:c.373_374insA	ENSP00000503416.1:p.Gly125GlufsTer?
ENST00000678555.1:c.373_374insA	ENSP00000504302.1:p.Gly125GlufsTer?
ENST00000678917.1:c.73_74insA	ENSP00000504428.1:p.Gly25GlufsTer?
ENST00000414423.6:c.73_74insA	ENSP00000408108.2:p.Gly25GlufsTer?
ENST00000445239.1:c.-20+1684_-20+1685insA	ENSP00000403597.1:n.-20+1684_-20+1685insA...
ENST00000486652.5:c.49_50insA	ENSP00000422758.1:p.Gly17GlufsTer?
NM_001115113.2:c.73_74insA	NP_001108585.2:p.Gly25GlufsTer?
NM_025160.6:c.73_74insA	NP_079436.4:p.Gly25GlufsTer?
XM_005273273.3:c.73_74insA	XP_005273330.1:p.Gly25GlufsTer?
XM_006711817.2:c.73_74insA	XP_006711880.1:p.Gly25GlufsTer?
XM_011544280.1:c.73_74insA	XP_011542582.1:p.Gly25GlufsTer?
XR_247043.2:n.165_166insA
XM_005273273.5:c.73_74insA	XP_005273330.1:p.Gly25GlufsTer?
XM_006711817.4:c.73_74insA	XP_006711880.1:p.Gly25GlufsTer?
XR_001737437.2:n.431_432insA
XR_002957642.1:n.431_432insA
XR_002957643.1:n.431_432insA
XR_002957644.1:n.735_736insA
XR_247043.4:n.431_432insA
NM_001115113.3:c.73_74insA	NP_001108585.2:p.Gly25GlufsTer?
NM_001379403.1:c.373_374insA MANE Select	NP_001366332.1:p.Gly125GlufsTer?
NM_025160.7:c.73_74insA	NP_079436.4:p.Gly25GlufsTer?