Canonical Allele Identifier: CA8620636

Gene: WNT3 LRRC37A2

Linked Data

• dbSNP Id: rs757175159
• ExAC: 17:44851014 CCT / C
• gnomAD v2: 17-44851014-CCT-C
• gnomAD v4: 17-46773648-CCT-C
• MyVariant Identifiers: chr17:g.44851015_44851016del (hg19) ; chr17:g.46773649_46773650del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773650_46773651del , CM000679.2:g.46773650_46773651del	GRCh38
NC_000017.10:g.44851016_44851017del , CM000679.1:g.44851016_44851017del	GRCh37
NC_000017.9:g.42206179_42206180del	NCBI36
NG_008084.2:g.50067_50068del

Transcript Alleles

HGVS	Amino-acid change
ENST00000706495.1:c.127+18_127+19del (WNT3)	ENSP00000516418.1:n.127+18_127+19del
ENST00000225512.6:c.322+18_322+19del (WNT3) MANE Select	ENSP00000225512.5:n.322+18_322+19del
ENST00000225512.5:c.322+18_322+19del (WNT3)	ENSP00000225512.5:n.322+18_322+19del
NM_030753.4:c.322+18_322+19del (WNT3)	NP_110380.1:n.322+18_322+19del
XM_024450773.1:c.4809+223131_4809+223132del (LRRC37A2)	XP_024306541.1:n.4809+223131_4809+223132d...
NM_030753.5:c.322+18_322+19del (WNT3) MANE Select	NP_110380.1:n.322+18_322+19del