Canonical Allele Identifier: CA2794284627

Gene: WNT5B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1633204G>A , CM000674.2:g.1633204G>A	GRCh38
NC_000012.11:g.1742370G>A , CM000674.1:g.1742370G>A	GRCh37
NC_000012.10:g.1612631G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397196.7:c.328+299G>A MANE Select	ENSP00000380379.2:n.328+299G>A
ENST00000310594.7:c.328+299G>A	ENSP00000308887.3:n.328+299G>A
ENST00000397196.6:c.328+299G>A	ENSP00000380379.2:n.328+299G>A
ENST00000537031.5:c.328+299G>A	ENSP00000439312.1:n.328+299G>A
ENST00000539198.5:c.328+299G>A	ENSP00000438414.1:n.328+299G>A
ENST00000542408.1:c.328+299G>A	ENSP00000440600.1:n.328+299G>A
ENST00000543071.5:c.328+299G>A	ENSP00000442348.1:n.328+299G>A
ENST00000545811.5:c.328+299G>A	ENSP00000445395.1:n.328+299G>A
NM_030775.2:c.328+299G>A	NP_110402.2:n.328+299G>A
NM_032642.2:c.328+299G>A	NP_116031.1:n.328+299G>A
XM_011521026.1:c.328+299G>A	XP_011519328.1:n.328+299G>A
XM_024449203.1:c.484+299G>A	XP_024304971.1:n.484+299G>A
XM_024449204.1:c.391+299G>A	XP_024304972.1:n.391+299G>A
XM_024449205.1:c.328+299G>A	XP_024304973.1:n.328+299G>A
XM_024449206.1:c.328+299G>A	XP_024304974.1:n.328+299G>A
XM_024449207.1:c.328+299G>A	XP_024304975.1:n.328+299G>A
XM_024449208.1:c.328+299G>A	XP_024304976.1:n.328+299G>A
XM_024449209.1:c.328+299G>A	XP_024304977.1:n.328+299G>A
NM_032642.3:c.328+299G>A MANE Select	NP_116031.1:n.328+299G>A