Canonical Allele Identifier: CA74909570

Gene: WNT5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.55486991G>T , CM000665.2:g.55486991G>T	GRCh38
NC_000003.11:g.55521019G>T , CM000665.1:g.55521019G>T	GRCh37
NC_000003.10:g.55496059G>T	NCBI36
NG_031992.1:g.5652C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264634.9:c.-6C>A MANE Select	ENSP00000264634.4:n.-6C>A
ENST00000264634.8:c.-6C>A	ENSP00000264634.4:n.-6C>A
ENST00000474267.5:c.-6C>A	ENSP00000417310.1:n.-6C>A
NM_003392.4:c.-6C>A	NP_003383.2:n.-6C>A
XM_011534081.1:c.-40+2846C>A	XP_011532383.1:n.-40+2846C>A
XM_011534082.1:c.-40+3039C>A	XP_011532384.1:n.-40+3039C>A
XM_011534083.1:c.-40+3039C>A	XP_011532385.1:n.-40+3039C>A
XM_011534084.1:c.-40+3039C>A	XP_011532386.1:n.-40+3039C>A
XM_011534085.1:c.-40+3039C>A	XP_011532387.1:n.-40+3039C>A
XM_011534086.1:c.-40+3039C>A	XP_011532388.1:n.-40+3039C>A
XM_011534085.2:c.-40+3039C>A	XP_011532387.1:n.-40+3039C>A
XM_011534086.2:c.-40+3039C>A	XP_011532388.1:n.-40+3039C>A
XM_017007127.1:c.48+1941C>A	XP_016862616.1:n.48+1941C>A
XM_017007128.1:c.-40+3039C>A	XP_016862617.1:n.-40+3039C>A
NM_003392.5:c.-51C>A	NP_003383.3:n.-51C>A
NM_003392.7:c.-6C>A MANE Select	NP_003383.4:n.-6C>A