Canonical Allele Identifier: CA596343654

Gene: WDR11

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.120874196_120874208del , CM000672.2:g.120874196_120874208del	GRCh38
NC_000010.10:g.122633708_122633720del , CM000672.1:g.122633708_122633720del	GRCh37
NC_000010.9:g.122623698_122623710del	NCBI36
NG_023290.1:g.28022_28034del

Transcript Alleles

HGVS	Amino-acid Change
NM_018117.12:c.1556+273_1556+285del MANE Select	NP_060587.8:n.1556+273_1556+285del
ENST00000263461.11:c.1556+273_1556+285del MANE Select	ENSP00000263461.5:n.1556+273_1556+285del
NM_018117.11:c.1556+273_1556+285del	NP_060587.8:n.1556+273_1556+285del
ENST00000263461.10:c.1556+273_1556+285del	ENSP00000263461.5:n.1556+273_1556+285del
ENST00000497136.6:c.*75+273_*75+285del	ENSP00000474595.1:n.*75+273_*75+285del
ENST00000604220.5:n.361+273_361+285del
ENST00000604585.5:c.779+273_779+285del	ENSP00000474880.1:n.779+273_779+285del
ENST00000605543.5:c.*75+273_*75+285del	ENSP00000475076.1:n.*75+273_*75+285del
XM_005269962.1:c.779+273_779+285del	XP_005270019.1:n.779+273_779+285del
XM_005269963.1:c.779+273_779+285del	XP_005270020.1:n.779+273_779+285del
XM_005269963.2:c.779+273_779+285del	XP_005270020.1:n.779+273_779+285del
XM_005269964.1:c.143+273_143+285del	XP_005270021.1:n.143+273_143+285del
XM_017016397.1:c.1382+273_1382+285del	XP_016871886.1:n.1382+273_1382+285del
XM_017016398.1:c.779+273_779+285del	XP_016871887.1:n.779+273_779+285del
XM_017016399.1:c.269+273_269+285del	XP_016871888.1:n.269+273_269+285del
XM_017016400.2:c.1556+273_1556+285del	XP_016871889.1:n.1556+273_1556+285del
XM_024448075.1:c.143+273_143+285del	XP_024303843.1:n.143+273_143+285del
XR_001747136.2:n.1637+273_1637+285del
XR_001747137.2:n.1637+273_1637+285del
XR_428707.1:n.1693+273_1693+285del
XR_428707.3:n.1637+273_1637+285del
XR_945785.1:n.1693+273_1693+285del