Canonical Allele Identifier: CA351623327

Gene: WNT7A

Linked Data

• MyVariant Identifiers: chr3:g.13896241T>A (hg19) ; chr3:g.13854744T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854744T>A , CM000665.2:g.13854744T>A	GRCh38
NC_000003.11:g.13896241T>A , CM000665.1:g.13896241T>A	GRCh37
NC_000003.10:g.13871242T>A	NCBI36
NG_008088.1:g.30378A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285018.5:c.358A>T MANE Select	ENSP00000285018.4:p.Thr120Ser
ENST00000285018.4:c.358A>T	ENSP00000285018.4:p.Thr120Ser
NM_004625.3:c.358A>T	NP_004616.2:p.Thr120Ser
XM_011534090.1:c.157A>T	XP_011532392.1:p.Thr53Ser
XM_011534091.1:c.157A>T	XP_011532393.1:p.Thr53Ser
XM_011534091.2:c.157A>T	XP_011532393.1:p.Thr53Ser
NM_004625.4:c.358A>T MANE Select	NP_004616.2:p.Thr120Ser