Canonical Allele Identifier: CA338920587

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456154A>T (hg19) ; chr1:g.22129661A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129661A>T , CM000663.2:g.22129661A>T	GRCh38
NC_000001.10:g.22456154A>T , CM000663.1:g.22456154A>T	GRCh37
NC_000001.9:g.22328741A>T	NCBI36
NG_008974.1:g.18366T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.268T>A MANE Select	ENSP00000290167.5:p.Ser90Thr
ENST00000290167.10:c.268T>A	ENSP00000290167.5:p.Ser90Thr
ENST00000415567.1:c.191T>A
ENST00000441048.1:c.103T>A	ENSP00000388925.1:p.Ser35Thr
NM_030761.4:c.268T>A	NP_110388.2:p.Ser90Thr
XM_011541597.1:c.334T>A	XP_011539899.1:p.Ser112Thr
XM_011541598.1:c.103T>A	XP_011539900.1:p.Ser35Thr
XM_011541599.1:c.334T>A	XP_011539901.1:p.Ser112Thr
XM_011541597.2:c.334T>A	XP_011539899.1:p.Ser112Thr
XM_011541598.2:c.103T>A	XP_011539900.1:p.Ser35Thr
NM_030761.5:c.268T>A MANE Select	NP_110388.2:p.Ser90Thr