Canonical Allele Identifier: CA338921813

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456333T>A (hg19) ; chr1:g.22129840T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129840T>A , CM000663.2:g.22129840T>A	GRCh38
NC_000001.10:g.22456333T>A , CM000663.1:g.22456333T>A	GRCh37
NC_000001.9:g.22328920T>A	NCBI36
NG_008974.1:g.18187A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.89A>T MANE Select	ENSP00000290167.5:p.Lys30Met
ENST00000290167.10:c.89A>T	ENSP00000290167.5:p.Lys30Met
ENST00000415567.1:c.12A>T
ENST00000441048.1:c.-77A>T	ENSP00000388925.1:n.-77A>T
NM_030761.4:c.89A>T	NP_110388.2:p.Lys30Met
XM_011541597.1:c.155A>T	XP_011539899.1:p.Lys52Met
XM_011541598.1:c.-77A>T	XP_011539900.1:n.-77A>T
XM_011541599.1:c.155A>T	XP_011539901.1:p.Lys52Met
XM_011541597.2:c.155A>T	XP_011539899.1:p.Lys52Met
XM_011541598.2:c.-77A>T	XP_011539900.1:n.-77A>T
NM_030761.5:c.89A>T MANE Select	NP_110388.2:p.Lys30Met