Canonical Allele Identifier: CA416559168

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456170G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129677G>A , CM000663.2:g.22129677G>A	GRCh38
NC_000001.10:g.22456170G>A , CM000663.1:g.22456170G>A	GRCh37
NC_000001.9:g.22328757G>A	NCBI36
NG_008974.1:g.18350C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.252C>T MANE Select	ENSP00000290167.5:p.Asn84=
ENST00000290167.10:c.252C>T	ENSP00000290167.5:p.Asn84=
ENST00000415567.1:c.175C>T
ENST00000441048.1:c.87C>T	ENSP00000388925.1:p.Asn29=
NM_030761.4:c.252C>T	NP_110388.2:p.Asn84=
XM_011541597.1:c.318C>T	XP_011539899.1:p.Asn106=
XM_011541598.1:c.87C>T	XP_011539900.1:p.Asn29=
XM_011541599.1:c.318C>T	XP_011539901.1:p.Asn106=
XM_011541597.2:c.318C>T	XP_011539899.1:p.Asn106=
XM_011541598.2:c.87C>T	XP_011539900.1:p.Asn29=
NM_030761.5:c.252C>T MANE Select	NP_110388.2:p.Asn84=