Canonical Allele Identifier: CA416559236

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456221C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129728C>T , CM000663.2:g.22129728C>T	GRCh38
NC_000001.10:g.22456221C>T , CM000663.1:g.22456221C>T	GRCh37
NC_000001.9:g.22328808C>T	NCBI36
NG_008974.1:g.18299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.201G>A MANE Select	ENSP00000290167.5:p.Val67=
ENST00000290167.10:c.201G>A	ENSP00000290167.5:p.Val67=
ENST00000415567.1:c.124G>A
ENST00000441048.1:c.36G>A	ENSP00000388925.1:p.Val12=
NM_030761.4:c.201G>A	NP_110388.2:p.Val67=
XM_011541597.1:c.267G>A	XP_011539899.1:p.Val89=
XM_011541598.1:c.36G>A	XP_011539900.1:p.Val12=
XM_011541599.1:c.267G>A	XP_011539901.1:p.Val89=
XM_011541597.2:c.267G>A	XP_011539899.1:p.Val89=
XM_011541598.2:c.36G>A	XP_011539900.1:p.Val12=
NM_030761.5:c.201G>A MANE Select	NP_110388.2:p.Val67=