Canonical Allele Identifier: CA2034926182

Gene: WNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981457G= , CM000674.2:g.48981457G=	GRCh38
NC_000012.11:g.49375240G= , CM000674.1:g.49375240G=	GRCh37
NC_000012.10:g.47661507G=	NCBI36
NG_033141.1:g.8005G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000293549.4:c.930G= MANE Select	ENSP00000293549.3:p.Thr310=
ENST00000293549.3:c.930G=	ENSP00000293549.3:p.Thr310=
ENST00000613114.4:c.897G=	ENSP00000481240.1:p.Thr299=
NM_005430.3:c.930G=	NP_005421.1:p.Thr310=
NM_005430.4:c.930G= MANE Select	NP_005421.1:p.Thr310=