Canonical Allele Identifier: CA14464890

Gene: WNT3 LRRC37A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46770300G>C , CM000679.2:g.46770300G>C	GRCh38
NC_000017.10:g.44847666G>C , CM000679.1:g.44847666G>C	GRCh37
NC_000017.9:g.42202834G>C	NCBI36
NG_008084.2:g.53417C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_030753.5:c.323-252C>G (WNT3) MANE Select	NP_110380.1:n.323-252C>G
ENST00000225512.6:c.323-252C>G (WNT3) MANE Select	ENSP00000225512.5:n.323-252C>G
NM_030753.4:c.323-252C>G (WNT3)	NP_110380.1:n.323-252C>G
ENST00000225512.5:c.323-252C>G (WNT3)	ENSP00000225512.5:n.323-252C>G
ENST00000706483.1:c.-233-252C>G (WNT3)	ENSP00000516407.1:n.-233-252C>G
ENST00000706484.1:c.-233-252C>G (WNT3)	ENSP00000516408.1:n.-233-252C>G
ENST00000706485.1:c.-233-252C>G (WNT3)	ENSP00000516409.1:n.-233-252C>G
ENST00000706495.1:c.128-252C>G (WNT3)	ENSP00000516418.1:n.128-252C>G
XM_024450773.1:c.4809+219781G>C (LRRC37A2)	XP_024306541.1:n.4809+219781G>C