Canonical Allele Identifier: CA338920901

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456187G>A (hg19) ; chr1:g.22129694G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129694G>A , CM000663.2:g.22129694G>A	GRCh38
NC_000001.10:g.22456187G>A , CM000663.1:g.22456187G>A	GRCh37
NC_000001.9:g.22328774G>A	NCBI36
NG_008974.1:g.18333C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.235C>T MANE Select	ENSP00000290167.5:p.Gln79Ter
ENST00000290167.10:c.235C>T	ENSP00000290167.5:p.Gln79Ter
ENST00000415567.1:c.158C>T
ENST00000441048.1:c.70C>T	ENSP00000388925.1:p.Gln24Ter
NM_030761.4:c.235C>T	NP_110388.2:p.Gln79Ter
XM_011541597.1:c.301C>T	XP_011539899.1:p.Gln101Ter
XM_011541598.1:c.70C>T	XP_011539900.1:p.Gln24Ter
XM_011541599.1:c.301C>T	XP_011539901.1:p.Gln101Ter
XM_011541597.2:c.301C>T	XP_011539899.1:p.Gln101Ter
XM_011541598.2:c.70C>T	XP_011539900.1:p.Gln24Ter
NM_030761.5:c.235C>T MANE Select	NP_110388.2:p.Gln79Ter