Canonical Allele Identifier: CA1983666779

Gene: WNT11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76198575A= , CM000673.2:g.76198575A=	GRCh38
NC_000011.9:g.75909619A= , CM000673.1:g.75909619A=	GRCh37
NC_000011.8:g.75587267A=	NCBI36
NG_046931.1:g.20434T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004626.3:c.84-1857T= MANE Select	NP_004617.2:n.84-1857T=
ENST00000322563.8:c.84-1857T= MANE Select	ENSP00000325526.3:n.84-1857T=
NM_004626.2:c.84-1857T=	NP_004617.2:n.84-1857T=
ENST00000322563.7:c.84-1857T=	ENSP00000325526.3:n.84-1857T=
ENST00000621122.1:c.84-1857T=	ENSP00000483229.1:n.84-1857T=
XM_005274231.1:c.84-1857T=	XP_005274288.1:n.84-1857T=
XM_011545237.1:c.84-1857T=	XP_011543539.1:n.84-1857T=
XM_011545238.1:c.84-1857T=	XP_011543540.1:n.84-1857T=
XM_011545239.1:c.84-1857T=	XP_011543541.1:n.84-1857T=
XM_011545239.2:c.84-1857T=	XP_011543541.1:n.84-1857T=
XM_011545240.1:c.84-1857T=	XP_011543542.1:n.84-1857T=
XM_011545240.2:c.84-1857T=	XP_011543542.1:n.84-1857T=
XM_024448678.1:c.-260-1857T=	XP_024304446.1:n.-260-1857T=
XR_002957190.1:n.257-1857T=
XR_950037.1:n.175-1857T=