Canonical Allele Identifier: CA479704568

Gene: WNT1

Linked Data

• MyVariant Identifiers: chr12:g.49375387C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981604C>T , CM000674.2:g.48981604C>T	GRCh38
NC_000012.11:g.49375387C>T , CM000674.1:g.49375387C>T	GRCh37
NC_000012.10:g.47661654C>T	NCBI36
NG_033141.1:g.8152C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.1077C>T MANE Select	ENSP00000293549.3:p.Asn359=
ENST00000293549.3:c.1077C>T	ENSP00000293549.3:p.Asn359=
ENST00000613114.4:c.1044C>T	ENSP00000481240.1:p.Asn348=
NM_005430.3:c.1077C>T	NP_005421.1:p.Asn359=
NM_005430.4:c.1077C>T MANE Select	NP_005421.1:p.Asn359=