Canonical Allele Identifier: CA416559325

Gene: WNT4

Linked Data

• dbSNP Id: rs1645969584
• MyVariant Identifiers: chr1:g.22456329C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129836C>G , CM000663.2:g.22129836C>G	GRCh38
NC_000001.10:g.22456329C>G , CM000663.1:g.22456329C>G	GRCh37
NC_000001.9:g.22328916C>G	NCBI36
NG_008974.1:g.18191G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.93G>C MANE Select	ENSP00000290167.5:p.Leu31=
ENST00000290167.10:c.93G>C	ENSP00000290167.5:p.Leu31=
ENST00000415567.1:c.16G>C
ENST00000441048.1:c.-73G>C	ENSP00000388925.1:n.-73G>C
NM_030761.4:c.93G>C	NP_110388.2:p.Leu31=
XM_011541597.1:c.159G>C	XP_011539899.1:p.Leu53=
XM_011541598.1:c.-73G>C	XP_011539900.1:n.-73G>C
XM_011541599.1:c.159G>C	XP_011539901.1:p.Leu53=
XM_011541597.2:c.159G>C	XP_011539899.1:p.Leu53=
XM_011541598.2:c.-73G>C	XP_011539900.1:n.-73G>C
NM_030761.5:c.93G>C MANE Select	NP_110388.2:p.Leu31=