Canonical Allele Identifier: CA338921592

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456298T>A (hg19) ; chr1:g.22129805T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129805T>A , CM000663.2:g.22129805T>A	GRCh38
NC_000001.10:g.22456298T>A , CM000663.1:g.22456298T>A	GRCh37
NC_000001.9:g.22328885T>A	NCBI36
NG_008974.1:g.18222A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.124A>T MANE Select	ENSP00000290167.5:p.Thr42Ser
ENST00000290167.10:c.124A>T	ENSP00000290167.5:p.Thr42Ser
ENST00000415567.1:c.47A>T
ENST00000441048.1:c.-42A>T	ENSP00000388925.1:n.-42A>T
NM_030761.4:c.124A>T	NP_110388.2:p.Thr42Ser
XM_011541597.1:c.190A>T	XP_011539899.1:p.Thr64Ser
XM_011541598.1:c.-42A>T	XP_011539900.1:n.-42A>T
XM_011541599.1:c.190A>T	XP_011539901.1:p.Thr64Ser
XM_011541597.2:c.190A>T	XP_011539899.1:p.Thr64Ser
XM_011541598.2:c.-42A>T	XP_011539900.1:n.-42A>T
NM_030761.5:c.124A>T MANE Select	NP_110388.2:p.Thr42Ser