Canonical Allele Identifier: CA338921595

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456298T>C (hg19) ; chr1:g.22129805T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129805T>C , CM000663.2:g.22129805T>C	GRCh38
NC_000001.10:g.22456298T>C , CM000663.1:g.22456298T>C	GRCh37
NC_000001.9:g.22328885T>C	NCBI36
NG_008974.1:g.18222A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.124A>G MANE Select	ENSP00000290167.5:p.Thr42Ala
ENST00000290167.10:c.124A>G	ENSP00000290167.5:p.Thr42Ala
ENST00000415567.1:c.47A>G
ENST00000441048.1:c.-42A>G	ENSP00000388925.1:n.-42A>G
NM_030761.4:c.124A>G	NP_110388.2:p.Thr42Ala
XM_011541597.1:c.190A>G	XP_011539899.1:p.Thr64Ala
XM_011541598.1:c.-42A>G	XP_011539900.1:n.-42A>G
XM_011541599.1:c.190A>G	XP_011539901.1:p.Thr64Ala
XM_011541597.2:c.190A>G	XP_011539899.1:p.Thr64Ala
XM_011541598.2:c.-42A>G	XP_011539900.1:n.-42A>G
NM_030761.5:c.124A>G MANE Select	NP_110388.2:p.Thr42Ala