Canonical Allele Identifier: CA338921869

Gene: WNT4

Linked Data

• dbSNP Id: rs1306215649
• gnomAD v2: 1-22456343-A-G
• gnomAD v4: 1-22129850-A-G
• MyVariant Identifiers: chr1:g.22456343A>G (hg19) ; chr1:g.22129850A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129850A>G , CM000663.2:g.22129850A>G	GRCh38
NC_000001.10:g.22456343A>G , CM000663.1:g.22456343A>G	GRCh37
NC_000001.9:g.22328930A>G	NCBI36
NG_008974.1:g.18177T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.79T>C MANE Select	ENSP00000290167.5:p.Tyr27His
ENST00000290167.10:c.79T>C	ENSP00000290167.5:p.Tyr27His
ENST00000415567.1:c.2T>C
ENST00000441048.1:c.-87T>C	ENSP00000388925.1:n.-87T>C
NM_030761.4:c.79T>C	NP_110388.2:p.Tyr27His
XM_011541597.1:c.145T>C	XP_011539899.1:p.Tyr49His
XM_011541598.1:c.-87T>C	XP_011539900.1:n.-87T>C
XM_011541599.1:c.145T>C	XP_011539901.1:p.Tyr49His
XM_011541597.2:c.145T>C	XP_011539899.1:p.Tyr49His
XM_011541598.2:c.-87T>C	XP_011539900.1:n.-87T>C
NM_030761.5:c.79T>C MANE Select	NP_110388.2:p.Tyr27His