Canonical Allele Identifier: CA416559327

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456332C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129839C>T , CM000663.2:g.22129839C>T	GRCh38
NC_000001.10:g.22456332C>T , CM000663.1:g.22456332C>T	GRCh37
NC_000001.9:g.22328919C>T	NCBI36
NG_008974.1:g.18188G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.90G>A MANE Select	ENSP00000290167.5:p.Lys30=
ENST00000290167.10:c.90G>A	ENSP00000290167.5:p.Lys30=
ENST00000415567.1:c.13G>A
ENST00000441048.1:c.-76G>A	ENSP00000388925.1:n.-76G>A
NM_030761.4:c.90G>A	NP_110388.2:p.Lys30=
XM_011541597.1:c.156G>A	XP_011539899.1:p.Lys52=
XM_011541598.1:c.-76G>A	XP_011539900.1:n.-76G>A
XM_011541599.1:c.156G>A	XP_011539901.1:p.Lys52=
XM_011541597.2:c.156G>A	XP_011539899.1:p.Lys52=
XM_011541598.2:c.-76G>A	XP_011539900.1:n.-76G>A
NM_030761.5:c.90G>A MANE Select	NP_110388.2:p.Lys30=