Canonical Allele Identifier: CA5720308

Gene: WDR11

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.120905947C>G , CM000672.2:g.120905947C>G	GRCh38
NC_000010.10:g.122665459C>G , CM000672.1:g.122665459C>G	GRCh37
NC_000010.9:g.122655449C>G	NCBI36
NG_023290.1:g.59773C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263461.11:c.3363C>G MANE Select	ENSP00000263461.5:p.Val1121=
ENST00000263461.10:c.3363C>G	ENSP00000263461.5:p.Val1121=
ENST00000497136.6:c.*1882C>G	ENSP00000474595.1:n.*1882C>G
ENST00000604509.5:n.3792C>G
ENST00000605543.5:c.*1882C>G	ENSP00000475076.1:n.*1882C>G
NM_018117.11:c.3363C>G	NP_060587.8:p.Val1121=
XM_005269962.1:c.2586C>G	XP_005270019.1:p.Val862=
XM_005269963.1:c.2586C>G	XP_005270020.1:p.Val862=
XM_005269964.1:c.1950C>G	XP_005270021.1:p.Val650=
XR_428707.1:n.3428+531C>G
XR_946372.1:n.253-3605G>C
XM_005269963.2:c.2586C>G	XP_005270020.1:p.Val862=
XM_017016397.1:c.3189C>G	XP_016871886.1:p.Val1063=
XM_017016398.1:c.2586C>G	XP_016871887.1:p.Val862=
XM_017016399.1:c.2076C>G	XP_016871888.1:p.Val692=
XM_024448075.1:c.1950C>G	XP_024303843.1:p.Val650=
XR_001747136.2:n.3272C>G
XR_001747137.2:n.3200+531C>G
XR_001747609.1:n.541-3605G>C
XR_428707.3:n.3372+531C>G
XR_946372.2:n.1156-3605G>C
NM_018117.12:c.3363C>G MANE Select	NP_060587.8:p.Val1121=