Canonical Allele Identifier: CA772510206

Gene: WNT3 LRRC37A2

Linked Data

• dbSNP Id: rs1396396263
• MyVariant Identifiers: chr17:g.44851352_44851353insG (hg19) ; chr17:g.46773986_46773987insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773986_46773987insG , CM000679.2:g.46773986_46773987insG	GRCh38
NC_000017.10:g.44851352_44851353insG , CM000679.1:g.44851352_44851353insG	GRCh37
NC_000017.9:g.42206515_42206516insG	NCBI36
NG_008084.2:g.49730_49731insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-115-78_-115-77insC (WNT3)	ENSP00000516418.1:n.-115-78_-115-77insC
ENST00000225512.6:c.81-78_81-77insC (WNT3) MANE Select	ENSP00000225512.5:n.81-78_81-77insC
ENST00000225512.5:c.81-78_81-77insC (WNT3)	ENSP00000225512.5:n.81-78_81-77insC
ENST00000573788.5:n.492-78_492-77insC (WNT3)
NM_030753.4:c.81-78_81-77insC (WNT3)	NP_110380.1:n.81-78_81-77insC
XM_024450773.1:c.4809+223467_4809+223468insG (LRRC37A2)	XP_024306541.1:n.4809+223467_4809+223468insG
NM_030753.5:c.81-78_81-77insC (WNT3) MANE Select	NP_110380.1:n.81-78_81-77insC