Canonical Allele Identifier: CA400011652

Gene: WNT3 LRRC37A2

Linked Data

• MyVariant Identifiers: chr17:g.44851267G>T (hg19) ; chr17:g.46773901G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773901G>T , CM000679.2:g.46773901G>T	GRCh38
NC_000017.10:g.44851267G>T , CM000679.1:g.44851267G>T	GRCh37
NC_000017.9:g.42206430G>T	NCBI36
NG_008084.2:g.49816C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-107C>A (WNT3)	ENSP00000516418.1:n.-107C>A
ENST00000225512.6:c.89C>A (WNT3) MANE Select	ENSP00000225512.5:p.Ala30Asp
ENST00000225512.5:c.89C>A (WNT3)	ENSP00000225512.5:p.Ala30Asp
ENST00000573788.5:n.500C>A (WNT3)
NM_030753.4:c.89C>A (WNT3)	NP_110380.1:p.Ala30Asp
XM_024450773.1:c.4809+223382G>T (LRRC37A2)	XP_024306541.1:n.4809+223382G>T
NM_030753.5:c.89C>A (WNT3) MANE Select	NP_110380.1:p.Ala30Asp