Canonical Allele Identifier: CA5719860

Gene: WDR11

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.120885864A>T , CM000672.2:g.120885864A>T	GRCh38
NC_000010.10:g.122645376A>T , CM000672.1:g.122645376A>T	GRCh37
NC_000010.9:g.122635366A>T	NCBI36
NG_023290.1:g.39690A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263461.11:c.1899A>T MANE Select	ENSP00000263461.5:p.Ala633=
ENST00000263461.10:c.1899A>T	ENSP00000263461.5:p.Ala633=
ENST00000497136.6:c.*418A>T	ENSP00000474595.1:n.*418A>T
ENST00000604509.5:n.1794A>T
ENST00000605376.5:n.167A>T
ENST00000605543.5:c.*418A>T	ENSP00000475076.1:n.*418A>T
NM_018117.11:c.1899A>T	NP_060587.8:p.Ala633=
XM_005269962.1:c.1122A>T	XP_005270019.1:p.Ala374=
XM_005269963.1:c.1122A>T	XP_005270020.1:p.Ala374=
XM_005269964.1:c.486A>T	XP_005270021.1:p.Ala162=
XR_428707.1:n.2036A>T
XR_945785.1:n.2036A>T
XM_005269963.2:c.1122A>T	XP_005270020.1:p.Ala374=
XM_017016397.1:c.1725A>T	XP_016871886.1:p.Ala575=
XM_017016398.1:c.1122A>T	XP_016871887.1:p.Ala374=
XM_017016399.1:c.612A>T	XP_016871888.1:p.Ala204=
XM_017016400.2:c.1899A>T	XP_016871889.1:p.Ala633=
XM_024448075.1:c.486A>T	XP_024303843.1:p.Ala162=
XR_001747136.2:n.1980A>T
XR_001747137.2:n.1980A>T
XR_428707.3:n.1980A>T
NM_018117.12:c.1899A>T MANE Select	NP_060587.8:p.Ala633=