Canonical Allele Identifier: CA338921779

Gene: WNT4

Linked Data

• gnomAD v4: 1-22129834-G-C
• MyVariant Identifiers: chr1:g.22456327G>C (hg19) ; chr1:g.22129834G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129834G>C , CM000663.2:g.22129834G>C	GRCh38
NC_000001.10:g.22456327G>C , CM000663.1:g.22456327G>C	GRCh37
NC_000001.9:g.22328914G>C	NCBI36
NG_008974.1:g.18193C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.95C>G MANE Select	ENSP00000290167.5:p.Ser32Trp
ENST00000290167.10:c.95C>G	ENSP00000290167.5:p.Ser32Trp
ENST00000415567.1:c.18C>G
ENST00000441048.1:c.-71C>G	ENSP00000388925.1:n.-71C>G
NM_030761.4:c.95C>G	NP_110388.2:p.Ser32Trp
XM_011541597.1:c.161C>G	XP_011539899.1:p.Ser54Trp
XM_011541598.1:c.-71C>G	XP_011539900.1:n.-71C>G
XM_011541599.1:c.161C>G	XP_011539901.1:p.Ser54Trp
XM_011541597.2:c.161C>G	XP_011539899.1:p.Ser54Trp
XM_011541598.2:c.-71C>G	XP_011539900.1:n.-71C>G
NM_030761.5:c.95C>G MANE Select	NP_110388.2:p.Ser32Trp