Canonical Allele Identifier: CA1557030888

Gene: WDR41

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.77485646A>G , CM000667.2:g.77485646A>G	GRCh38
NC_000005.9:g.76781471A>G , CM000667.1:g.76781471A>G	GRCh37
NC_000005.8:g.76817227A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296679.9:c.167+3811T>C MANE Select	ENSP00000296679.4:n.167+3811T>C
ENST00000296679.8:c.167+3811T>C	ENSP00000296679.4:n.167+3811T>C
ENST00000414719.6:c.167+3811T>C	ENSP00000392931.3:n.167+3811T>C
ENST00000503035.5:c.*94+3811T>C	ENSP00000421166.1:n.*94+3811T>C
ENST00000504895.5:c.143+3811T>C	ENSP00000426141.1:n.143+3811T>C
ENST00000505129.5:c.167+3811T>C	ENSP00000425249.1:n.167+3811T>C
ENST00000506307.5:c.167+3811T>C	ENSP00000424327.1:n.167+3811T>C
ENST00000506474.5:c.167+3811T>C	ENSP00000425813.1:n.167+3811T>C
ENST00000507029.5:c.51+6524T>C	ENSP00000424287.1:n.51+6524T>C
ENST00000507239.5:n.169+3811T>C
ENST00000507452.5:n.162+3811T>C
ENST00000507654.5:c.10+3811T>C	ENSP00000427291.1:n.10+3811T>C
ENST00000509701.5:c.167+3811T>C	ENSP00000427652.1:n.167+3811T>C
ENST00000509858.5:n.278+3811T>C
ENST00000509892.5:c.162+3811T>C
ENST00000509971.5:c.158+3811T>C	ENSP00000422922.1:n.158+3811T>C
ENST00000511036.5:c.152+3811T>C	ENSP00000422510.1:n.152+3811T>C
ENST00000511791.1:c.73+3905T>C	ENSP00000423540.1:n.73+3905T>C
ENST00000512168.1:n.397+3811T>C
ENST00000513417.5:c.167+3811T>C	ENSP00000423462.1:n.167+3811T>C
ENST00000513917.5:n.426+3811T>C
ENST00000514451.5:n.293+3811T>C
ENST00000514559.5:c.167+3811T>C	ENSP00000426937.1:n.167+3811T>C
ENST00000515253.5:c.146+3811T>C	ENSP00000426499.1:n.146+3811T>C
ENST00000515321.5:n.168+3811T>C
NM_018268.2:c.167+3811T>C	NP_060738.2:n.167+3811T>C
XM_005248551.3:c.167+3811T>C	XP_005248608.1:n.167+3811T>C
XM_005248552.2:c.167+3811T>C	XP_005248609.1:n.167+3811T>C
XM_006714656.2:c.167+3811T>C	XP_006714719.1:n.167+3811T>C
XM_011543505.1:c.158+3811T>C	XP_011541807.1:n.158+3811T>C
XM_011543506.1:c.12-20837T>C	XP_011541808.1:n.12-20837T>C
XM_011543507.1:c.167+3811T>C	XP_011541809.1:n.167+3811T>C
NM_018268.3:c.167+3811T>C	NP_060738.2:n.167+3811T>C
XM_005248551.4:c.167+3811T>C	XP_005248608.1:n.167+3811T>C
XM_005248552.3:c.167+3811T>C	XP_005248609.1:n.167+3811T>C
XM_011543505.2:c.158+3811T>C	XP_011541807.1:n.158+3811T>C
XM_011543507.2:c.167+3811T>C	XP_011541809.1:n.167+3811T>C
XM_017009606.1:c.155+3811T>C	XP_016865095.1:n.155+3811T>C
XR_001742140.1:n.454+3811T>C
XR_001742141.1:n.454+3811T>C
NM_018268.4:c.167+3811T>C MANE Select	NP_060738.2:n.167+3811T>C