Canonical Allele Identifier: CA338921685

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456313T>A (hg19) ; chr1:g.22129820T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129820T>A , CM000663.2:g.22129820T>A	GRCh38
NC_000001.10:g.22456313T>A , CM000663.1:g.22456313T>A	GRCh37
NC_000001.9:g.22328900T>A	NCBI36
NG_008974.1:g.18207A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.109A>T MANE Select	ENSP00000290167.5:p.Ile37Phe
ENST00000290167.10:c.109A>T	ENSP00000290167.5:p.Ile37Phe
ENST00000415567.1:c.32A>T
ENST00000441048.1:c.-57A>T	ENSP00000388925.1:n.-57A>T
NM_030761.4:c.109A>T	NP_110388.2:p.Ile37Phe
XM_011541597.1:c.175A>T	XP_011539899.1:p.Ile59Phe
XM_011541598.1:c.-57A>T	XP_011539900.1:n.-57A>T
XM_011541599.1:c.175A>T	XP_011539901.1:p.Ile59Phe
XM_011541597.2:c.175A>T	XP_011539899.1:p.Ile59Phe
XM_011541598.2:c.-57A>T	XP_011539900.1:n.-57A>T
NM_030761.5:c.109A>T MANE Select	NP_110388.2:p.Ile37Phe