Canonical Allele Identifier: CA2742784997

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129968_22129969insTCCTGGGGCCCCCAAC , CM000663.2:g.22129968_22129969insTCCTGGGGCCCCCAAC	GRCh38
NC_000001.10:g.22456461_22456462insTCCTGGGGCCCCCAAC , CM000663.1:g.22456461_22456462insTCCTGGGGCCCCCAAC	GRCh37
NC_000001.9:g.22329048_22329049insTCCTGGGGCCCCCAAC	NCBI36
NG_008974.1:g.18058_18059insGTTGGGGGCCCCAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.78-118_78-117insGTTGGGGGCCCCAGGA MANE Select	ENSP00000290167.5:n.78-118_78-117insGTTGGGGGCCCCAGGA
ENST00000290167.10:c.78-118_78-117insGTTGGGGGCCCCAGGA	ENSP00000290167.5:n.78-118_78-117insGTTGGGGGCCCCAGGA
ENST00000441048.1:c.-88-118_-88-117insGTTGGGGGCCCCAGGA	ENSP00000388925.1:n.-88-118_-88-117insGTTGGGGGCCCCAGGA
NM_030761.4:c.78-118_78-117insGTTGGGGGCCCCAGGA	NP_110388.2:n.78-118_78-117insGTTGGGGGCCCCAGGA
XM_011541597.1:c.144-118_144-117insGTTGGGGGCCCCAGGA	XP_011539899.1:n.144-118_144-117insGTTGGGGGCCCCAGGA
XM_011541598.1:c.-88-118_-88-117insGTTGGGGGCCCCAGGA	XP_011539900.1:n.-88-118_-88-117insGTTGGGGGCCCCAGGA
XM_011541599.1:c.144-118_144-117insGTTGGGGGCCCCAGGA	XP_011539901.1:n.144-118_144-117insGTTGGGGGCCCCAGGA
XM_011541597.2:c.144-118_144-117insGTTGGGGGCCCCAGGA	XP_011539899.1:n.144-118_144-117insGTTGGGGGCCCCAGGA
XM_011541598.2:c.-88-118_-88-117insGTTGGGGGCCCCAGGA	XP_011539900.1:n.-88-118_-88-117insGTTGGGGGCCCCAGGA
NM_030761.5:c.78-118_78-117insGTTGGGGGCCCCAGGA MANE Select	NP_110388.2:n.78-118_78-117insGTTGGGGGCCCCAGGA