Canonical Allele Identifier: CA353267394
Community Standard Title: NM_003392.7(WNT5A):c.248G>A (p.Cys83Tyr)
Gene: WNT5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.55479457C>T , CM000665.2:g.55479457C>T GRCh38
NC_000003.11:g.55513485C>T , CM000665.1:g.55513485C>T GRCh37
NC_000003.10:g.55488525C>T NCBI36
NG_031992.1:g.13186G>A

Transcript Alleles

HGVS Amino-acid Change
NM_003392.7:c.248G>A MANE Select NP_003383.4:p.Cys83Tyr
ENST00000264634.9:c.248G>A MANE Select ENSP00000264634.4:p.Cys83Tyr
NM_001256105.1:c.203G>A NP_001243034.1:p.Cys68Tyr
NM_001377271.1:c.203G>A NP_001364200.1:p.Cys68Tyr
NM_001377272.1:c.203G>A NP_001364201.1:p.Cys68Tyr
NM_003392.4:c.248G>A NP_003383.2:p.Cys83Tyr
NM_003392.5:c.203G>A NP_003383.3:p.Cys68Tyr
ENST00000264634.8:c.248G>A ENSP00000264634.4:p.Cys83Tyr
ENST00000474267.5:c.248G>A ENSP00000417310.1:p.Cys83Tyr
ENST00000482079.1:c.203G>A ENSP00000418184.1:p.Cys68Tyr
ENST00000497027.5:c.203G>A ENSP00000420104.1:p.Cys68Tyr
ENST00000497817.1:n.244G>A
ENST00000614415.1:c.177+71G>A ENSP00000478784.1:n.177+71G>A
XM_006713324.1:c.203G>A XP_006713387.1:p.Cys68Tyr
XM_011534081.1:c.203G>A XP_011532383.1:p.Cys68Tyr
XM_011534082.1:c.203G>A XP_011532384.1:p.Cys68Tyr
XM_011534083.1:c.203G>A XP_011532385.1:p.Cys68Tyr
XM_011534084.1:c.203G>A XP_011532386.1:p.Cys68Tyr
XM_011534085.1:c.203G>A XP_011532387.1:p.Cys68Tyr
XM_011534085.2:c.203G>A XP_011532387.1:p.Cys68Tyr
XM_011534086.1:c.203G>A XP_011532388.1:p.Cys68Tyr
XM_011534086.2:c.203G>A XP_011532388.1:p.Cys68Tyr
XM_011534087.1:c.203G>A XP_011532389.1:p.Cys68Tyr
XM_011534087.2:c.203G>A XP_011532389.1:p.Cys68Tyr
XM_011534088.1:c.203G>A XP_011532390.1:p.Cys68Tyr
XM_011534088.2:c.203G>A XP_011532390.1:p.Cys68Tyr
XM_011534089.1:c.203G>A XP_011532391.1:p.Cys68Tyr
XM_017007127.1:c.290G>A XP_016862616.1:p.Cys97Tyr
XM_017007128.1:c.203G>A XP_016862617.1:p.Cys68Tyr