Canonical Allele Identifier: CA338920799

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456177A>G (hg19) ; chr1:g.22129684A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129684A>G , CM000663.2:g.22129684A>G	GRCh38
NC_000001.10:g.22456177A>G , CM000663.1:g.22456177A>G	GRCh37
NC_000001.9:g.22328764A>G	NCBI36
NG_008974.1:g.18343T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.245T>C MANE Select	ENSP00000290167.5:p.Phe82Ser
ENST00000290167.10:c.245T>C	ENSP00000290167.5:p.Phe82Ser
ENST00000415567.1:c.168T>C
ENST00000441048.1:c.80T>C	ENSP00000388925.1:p.Phe27Ser
NM_030761.4:c.245T>C	NP_110388.2:p.Phe82Ser
XM_011541597.1:c.311T>C	XP_011539899.1:p.Phe104Ser
XM_011541598.1:c.80T>C	XP_011539900.1:p.Phe27Ser
XM_011541599.1:c.311T>C	XP_011539901.1:p.Phe104Ser
XM_011541597.2:c.311T>C	XP_011539899.1:p.Phe104Ser
XM_011541598.2:c.80T>C	XP_011539900.1:p.Phe27Ser
NM_030761.5:c.245T>C MANE Select	NP_110388.2:p.Phe82Ser