Canonical Allele Identifier: CA1158260837

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129800_22129807delinsGCACGTCT , CM000663.2:g.22129800_22129807delinsGCACGTCT	GRCh38
NC_000001.10:g.22456293_22456300delinsGCACGTCT , CM000663.1:g.22456293_22456300delinsGCACGTCT	GRCh37
NC_000001.9:g.22328880_22328887delinsGCACGTCT	NCBI36
NG_008974.1:g.18220_18227delinsAGACGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.122_129delinsAGACGTGC MANE Select	ENSP00000290167.5:p.Glu41=
ENST00000290167.10:c.122_129delinsAGACGTGC	ENSP00000290167.5:p.Glu41=
ENST00000415567.1:c.45_52delinsAGACGTGC
ENST00000441048.1:c.-44_-37delinsAGACGTGC	ENSP00000388925.1:n.-44_-37delinsAGACGTGC
NM_030761.4:c.122_129delinsAGACGTGC	NP_110388.2:p.Glu41=
XM_011541597.1:c.188_195delinsAGACGTGC	XP_011539899.1:p.Glu63=
XM_011541598.1:c.-44_-37delinsAGACGTGC	XP_011539900.1:n.-44_-37delinsAGACGTGC
XM_011541599.1:c.188_195delinsAGACGTGC	XP_011539901.1:p.Glu63=
XM_011541597.2:c.188_195delinsAGACGTGC	XP_011539899.1:p.Glu63=
XM_011541598.2:c.-44_-37delinsAGACGTGC	XP_011539900.1:n.-44_-37delinsAGACGTGC
NM_030761.5:c.122_129delinsAGACGTGC MANE Select	NP_110388.2:p.Glu41=