Canonical Allele Identifier: CA351623335

Gene: WNT7A

Linked Data

• MyVariant Identifiers: chr3:g.13896244T>C (hg19) ; chr3:g.13854747T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854747T>C , CM000665.2:g.13854747T>C	GRCh38
NC_000003.11:g.13896244T>C , CM000665.1:g.13896244T>C	GRCh37
NC_000003.10:g.13871245T>C	NCBI36
NG_008088.1:g.30375A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285018.5:c.355A>G MANE Select	ENSP00000285018.4:p.Ile119Val
ENST00000285018.4:c.355A>G	ENSP00000285018.4:p.Ile119Val
NM_004625.3:c.355A>G	NP_004616.2:p.Ile119Val
XM_011534090.1:c.154A>G	XP_011532392.1:p.Ile52Val
XM_011534091.1:c.154A>G	XP_011532393.1:p.Ile52Val
XM_011534091.2:c.154A>G	XP_011532393.1:p.Ile52Val
NM_004625.4:c.355A>G MANE Select	NP_004616.2:p.Ile119Val