Canonical Allele Identifier: CA5719917

Gene: WDR11

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.120886867A>G , CM000672.2:g.120886867A>G	GRCh38
NC_000010.10:g.122646379A>G , CM000672.1:g.122646379A>G	GRCh37
NC_000010.9:g.122636369A>G	NCBI36
NG_023290.1:g.40693A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263461.11:c.2121+31A>G MANE Select	ENSP00000263461.5:n.2121+31A>G
ENST00000263461.10:c.2121+31A>G	ENSP00000263461.5:n.2121+31A>G
ENST00000478567.5:n.219+31A>G
ENST00000497136.6:c.*640+31A>G	ENSP00000474595.1:n.*640+31A>G
ENST00000604509.5:n.2016+31A>G
ENST00000605376.5:n.389+31A>G
ENST00000605543.5:c.*640+31A>G	ENSP00000475076.1:n.*640+31A>G
NM_018117.11:c.2121+31A>G	NP_060587.8:n.2121+31A>G
XM_005269962.1:c.1344+31A>G	XP_005270019.1:n.1344+31A>G
XM_005269963.1:c.1344+31A>G	XP_005270020.1:n.1344+31A>G
XM_005269964.1:c.708+31A>G	XP_005270021.1:n.708+31A>G
XR_428707.1:n.2258+31A>G
XR_945785.1:n.2258+31A>G
XM_005269963.2:c.1344+31A>G	XP_005270020.1:n.1344+31A>G
XM_017016397.1:c.1947+31A>G	XP_016871886.1:n.1947+31A>G
XM_017016398.1:c.1344+31A>G	XP_016871887.1:n.1344+31A>G
XM_017016399.1:c.834+31A>G	XP_016871888.1:n.834+31A>G
XM_017016400.2:c.2121+31A>G	XP_016871889.1:n.2121+31A>G
XM_024448075.1:c.708+31A>G	XP_024303843.1:n.708+31A>G
XR_001747136.2:n.2202+31A>G
XR_001747137.2:n.2202+31A>G
XR_428707.3:n.2202+31A>G
NM_018117.12:c.2121+31A>G MANE Select	NP_060587.8:n.2121+31A>G