Canonical Allele Identifier: CA338920790

Gene: WNT4

Linked Data

• gnomAD v4: 1-22129683-G-T
• MyVariant Identifiers: chr1:g.22456176G>T (hg19) ; chr1:g.22129683G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129683G>T , CM000663.2:g.22129683G>T	GRCh38
NC_000001.10:g.22456176G>T , CM000663.1:g.22456176G>T	GRCh37
NC_000001.9:g.22328763G>T	NCBI36
NG_008974.1:g.18344C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.246C>A MANE Select	ENSP00000290167.5:p.Phe82Leu
ENST00000290167.10:c.246C>A	ENSP00000290167.5:p.Phe82Leu
ENST00000415567.1:c.169C>A
ENST00000441048.1:c.81C>A	ENSP00000388925.1:p.Phe27Leu
NM_030761.4:c.246C>A	NP_110388.2:p.Phe82Leu
XM_011541597.1:c.312C>A	XP_011539899.1:p.Phe104Leu
XM_011541598.1:c.81C>A	XP_011539900.1:p.Phe27Leu
XM_011541599.1:c.312C>A	XP_011539901.1:p.Phe104Leu
XM_011541597.2:c.312C>A	XP_011539899.1:p.Phe104Leu
XM_011541598.2:c.81C>A	XP_011539900.1:p.Phe27Leu
NM_030761.5:c.246C>A MANE Select	NP_110388.2:p.Phe82Leu