Canonical Allele Identifier: CA1158260893

Gene: WNT4

Linked Data

• dbSNP Id: rs1645970386

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129918_22129919insGGCCCCGGACC , CM000663.2:g.22129918_22129919insGGCCCCGGACC	GRCh38
NC_000001.10:g.22456411_22456412insGGCCCCGGACC , CM000663.1:g.22456411_22456412insGGCCCCGGACC	GRCh37
NC_000001.9:g.22328998_22328999insGGCCCCGGACC	NCBI36
NG_008974.1:g.18108_18109insGGTCCGGGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.78-68_78-67insGGTCCGGGGCC MANE Select	ENSP00000290167.5:n.78-68_78-67insGGTCCGGGGCC
ENST00000290167.10:c.78-68_78-67insGGTCCGGGGCC	ENSP00000290167.5:n.78-68_78-67insGGTCCGGGGCC
ENST00000441048.1:c.-88-68_-88-67insGGTCCGGGGCC	ENSP00000388925.1:n.-88-68_-88-67insGGTCCGGGGCC
NM_030761.4:c.78-68_78-67insGGTCCGGGGCC	NP_110388.2:n.78-68_78-67insGGTCCGGGGCC
XM_011541597.1:c.144-68_144-67insGGTCCGGGGCC	XP_011539899.1:n.144-68_144-67insGGTCCGGGGCC
XM_011541598.1:c.-88-68_-88-67insGGTCCGGGGCC	XP_011539900.1:n.-88-68_-88-67insGGTCCGGGGCC
XM_011541599.1:c.144-68_144-67insGGTCCGGGGCC	XP_011539901.1:n.144-68_144-67insGGTCCGGGGCC
XM_011541597.2:c.144-68_144-67insGGTCCGGGGCC	XP_011539899.1:n.144-68_144-67insGGTCCGGGGCC
XM_011541598.2:c.-88-68_-88-67insGGTCCGGGGCC	XP_011539900.1:n.-88-68_-88-67insGGTCCGGGGCC
NM_030761.5:c.78-68_78-67insGGTCCGGGGCC MANE Select	NP_110388.2:n.78-68_78-67insGGTCCGGGGCC