Canonical Allele Identifier: CA2575143759

Gene: WNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981572_48981575del , CM000674.2:g.48981572_48981575del	GRCh38
NC_000012.11:g.49375355_49375358del , CM000674.1:g.49375355_49375358del	GRCh37
NC_000012.10:g.47661622_47661625del	NCBI36
NG_033141.1:g.8120_8123del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.1045_1048del MANE Select	ENSP00000293549.3:p.Phe349ThrfsTer?
ENST00000293549.3:c.1045_1048del	ENSP00000293549.3:p.Phe349ThrfsTer?
ENST00000613114.4:c.1012_1015del	ENSP00000481240.1:p.Phe338ThrfsTer?
NM_005430.3:c.1045_1048del	NP_005421.1:p.Phe349ThrfsTer?
NM_005430.4:c.1045_1048del MANE Select	NP_005421.1:p.Phe349ThrfsTer?