Canonical Allele Identifier: CA338921486

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456282T>G (hg19) ; chr1:g.22129789T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129789T>G , CM000663.2:g.22129789T>G	GRCh38
NC_000001.10:g.22456282T>G , CM000663.1:g.22456282T>G	GRCh37
NC_000001.9:g.22328869T>G	NCBI36
NG_008974.1:g.18238A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.140A>C MANE Select	ENSP00000290167.5:p.Lys47Thr
ENST00000290167.10:c.140A>C	ENSP00000290167.5:p.Lys47Thr
ENST00000415567.1:c.63A>C
ENST00000441048.1:c.-26A>C	ENSP00000388925.1:n.-26A>C
NM_030761.4:c.140A>C	NP_110388.2:p.Lys47Thr
XM_011541597.1:c.206A>C	XP_011539899.1:p.Lys69Thr
XM_011541598.1:c.-26A>C	XP_011539900.1:n.-26A>C
XM_011541599.1:c.206A>C	XP_011539901.1:p.Lys69Thr
XM_011541597.2:c.206A>C	XP_011539899.1:p.Lys69Thr
XM_011541598.2:c.-26A>C	XP_011539900.1:n.-26A>C
NM_030761.5:c.140A>C MANE Select	NP_110388.2:p.Lys47Thr