Canonical Allele Identifier: CA384637635

Gene: WNT1

Linked Data

• MyVariant Identifiers: chr12:g.49375277G>T (hg19) ; chr12:g.48981494G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981494G>T , CM000674.2:g.48981494G>T	GRCh38
NC_000012.11:g.49375277G>T , CM000674.1:g.49375277G>T	GRCh37
NC_000012.10:g.47661544G>T	NCBI36
NG_033141.1:g.8042G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.967G>T MANE Select	ENSP00000293549.3:p.Asp323Tyr
ENST00000293549.3:c.967G>T	ENSP00000293549.3:p.Asp323Tyr
ENST00000613114.4:c.934G>T	ENSP00000481240.1:p.Asp312Tyr
NM_005430.3:c.967G>T	NP_005421.1:p.Asp323Tyr
NM_005430.4:c.967G>T MANE Select	NP_005421.1:p.Asp323Tyr