Canonical Allele Identifier: CA338916628

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22446864C>G (hg19) ; chr1:g.22120371C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22120371C>G , CM000663.2:g.22120371C>G	GRCh38
NC_000001.10:g.22446864C>G , CM000663.1:g.22446864C>G	GRCh37
NC_000001.9:g.22319451C>G	NCBI36
NG_008974.1:g.27656G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.735G>C MANE Select	ENSP00000290167.5:p.Glu245Asp
ENST00000290167.10:c.735G>C	ENSP00000290167.5:p.Glu245Asp
NM_030761.4:c.735G>C	NP_110388.2:p.Glu245Asp
XM_011541597.1:c.801G>C	XP_011539899.1:p.Glu267Asp
XM_011541598.1:c.570G>C	XP_011539900.1:p.Glu190Asp
XM_011541597.2:c.801G>C	XP_011539899.1:p.Glu267Asp
XM_011541598.2:c.570G>C	XP_011539900.1:p.Glu190Asp
NM_030761.5:c.735G>C MANE Select	NP_110388.2:p.Glu245Asp