Canonical Allele Identifier: CA338921669

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456310A>C (hg19) ; chr1:g.22129817A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129817A>C , CM000663.2:g.22129817A>C	GRCh38
NC_000001.10:g.22456310A>C , CM000663.1:g.22456310A>C	GRCh37
NC_000001.9:g.22328897A>C	NCBI36
NG_008974.1:g.18210T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.112T>G MANE Select	ENSP00000290167.5:p.Ser38Ala
ENST00000290167.10:c.112T>G	ENSP00000290167.5:p.Ser38Ala
ENST00000415567.1:c.35T>G
ENST00000441048.1:c.-54T>G	ENSP00000388925.1:n.-54T>G
NM_030761.4:c.112T>G	NP_110388.2:p.Ser38Ala
XM_011541597.1:c.178T>G	XP_011539899.1:p.Ser60Ala
XM_011541598.1:c.-54T>G	XP_011539900.1:n.-54T>G
XM_011541599.1:c.178T>G	XP_011539901.1:p.Ser60Ala
XM_011541597.2:c.178T>G	XP_011539899.1:p.Ser60Ala
XM_011541598.2:c.-54T>G	XP_011539900.1:n.-54T>G
NM_030761.5:c.112T>G MANE Select	NP_110388.2:p.Ser38Ala