Canonical Allele Identifier: CA291159636

Gene: WNT3 LRRC37A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46768172C>T , CM000679.2:g.46768172C>T	GRCh38
NC_000017.10:g.44845538C>T , CM000679.1:g.44845538C>T	GRCh37
NC_000017.9:g.42200707C>T	NCBI36
NG_008084.2:g.55545G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706483.1:c.*8+140G>A (WNT3)	ENSP00000516407.1:n.*8+140G>A
ENST00000706484.1:c.*494+140G>A (WNT3)	ENSP00000516408.1:n.*494+140G>A
ENST00000706485.1:c.*8+140G>A (WNT3)	ENSP00000516409.1:n.*8+140G>A
ENST00000706495.1:c.*8+140G>A (WNT3)	ENSP00000516418.1:n.*8+140G>A
ENST00000225512.6:c.*8+140G>A (WNT3) MANE Select	ENSP00000225512.5:n.*8+140G>A
ENST00000225512.5:c.*8+140G>A (WNT3)	ENSP00000225512.5:n.*8+140G>A
NM_030753.4:c.*8+140G>A (WNT3)	NP_110380.1:n.*8+140G>A
XM_024450773.1:c.4809+217653C>T (LRRC37A2)	XP_024306541.1:n.4809+217653C>T
NM_030753.5:c.*8+140G>A (WNT3) MANE Select	NP_110380.1:n.*8+140G>A