Canonical Allele Identifier: CA10616460

Gene: WNT5A

Linked Data

• ClinVar Variation Id: 346231
• ClinVar RCV Id: RCV000339679
• dbSNP Id: rs760058727
• gnomAD v2: 3-55501406-TTTG-T
• gnomAD v3: 3-55467378-TTTG-T
• gnomAD v4: 3-55467378-TTTG-T
• MyVariant Identifiers: chr3:g.55501407_55501409del (hg19) ; chr3:g.55467379_55467381del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.55467380_55467382del , CM000665.2:g.55467380_55467382del	GRCh38
NC_000003.11:g.55501408_55501410del , CM000665.1:g.55501408_55501410del	GRCh37
NC_000003.10:g.55476448_55476450del	NCBI36
NG_031992.1:g.25262_25264del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264634.9:c.*2711_*2713del MANE Select	ENSP00000264634.4:n.*2711_*2713del
ENST00000264634.8:c.*2711_*2713del	ENSP00000264634.4:n.*2711_*2713del
ENST00000474267.5:c.*2711_*2713del	ENSP00000417310.1:n.*2711_*2713del
NM_001256105.1:c.*2711_*2713del	NP_001243034.1:n.*2711_*2713del
NM_003392.4:c.*2711_*2713del	NP_003383.2:n.*2711_*2713del
XM_006713324.1:c.*2711_*2713del	XP_006713387.1:n.*2711_*2713del
XM_011534081.1:c.*2711_*2713del	XP_011532383.1:n.*2711_*2713del
XM_011534082.1:c.*2711_*2713del	XP_011532384.1:n.*2711_*2713del
XM_011534083.1:c.*2711_*2713del	XP_011532385.1:n.*2711_*2713del
XM_011534084.1:c.*2711_*2713del	XP_011532386.1:n.*2711_*2713del
XM_011534085.1:c.*2711_*2713del	XP_011532387.1:n.*2711_*2713del
XM_011534086.1:c.*2711_*2713del	XP_011532388.1:n.*2711_*2713del
XM_011534087.1:c.*2711_*2713del	XP_011532389.1:n.*2711_*2713del
XM_011534088.1:c.*2711_*2713del	XP_011532390.1:n.*2711_*2713del
XM_011534089.1:c.*2711_*2713del	XP_011532391.1:n.*2711_*2713del
XM_011534085.2:c.*2711_*2713del	XP_011532387.1:n.*2711_*2713del
XM_011534086.2:c.*2711_*2713del	XP_011532388.1:n.*2711_*2713del
XM_011534087.2:c.*2711_*2713del	XP_011532389.1:n.*2711_*2713del
XM_011534088.2:c.*2711_*2713del	XP_011532390.1:n.*2711_*2713del
XM_017007127.1:c.*2711_*2713del	XP_016862616.1:n.*2711_*2713del
XM_017007128.1:c.*2711_*2713del	XP_016862617.1:n.*2711_*2713del
NM_001377271.1:c.*2711_*2713del	NP_001364200.1:n.*2711_*2713del
NM_001377272.1:c.*2711_*2713del	NP_001364201.1:n.*2711_*2713del
NM_003392.5:c.*2711_*2713del	NP_003383.3:n.*2711_*2713del
NM_003392.7:c.*2711_*2713del MANE Select	NP_003383.4:n.*2711_*2713del