Canonical Allele Identifier: CA11361841

Gene: WNT5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.55487689C>A , CM000665.2:g.55487689C>A	GRCh38
NC_000003.11:g.55521717C>A , CM000665.1:g.55521717C>A	GRCh37
NC_000003.10:g.55496757C>A	NCBI36
NG_031992.1:g.4954G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474267.5:c.-413-291G>T	ENSP00000417310.1:n.-413-291G>T
XM_011534081.1:c.-40+2148G>T	XP_011532383.1:n.-40+2148G>T
XM_011534082.1:c.-40+2341G>T	XP_011532384.1:n.-40+2341G>T
XM_011534083.1:c.-40+2341G>T	XP_011532385.1:n.-40+2341G>T
XM_011534084.1:c.-40+2341G>T	XP_011532386.1:n.-40+2341G>T
XM_011534085.1:c.-40+2341G>T	XP_011532387.1:n.-40+2341G>T
XM_011534085.2:c.-40+2341G>T	XP_011532387.1:n.-40+2341G>T
XM_011534086.1:c.-40+2341G>T	XP_011532388.1:n.-40+2341G>T
XM_011534086.2:c.-40+2341G>T	XP_011532388.1:n.-40+2341G>T
XM_017007127.1:c.48+1243G>T	XP_016862616.1:n.48+1243G>T
XM_017007128.1:c.-40+2341G>T	XP_016862617.1:n.-40+2341G>T