Canonical Allele Identifier: CA16539999

Gene: WNT3 LRRC37A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46768080A>G , CM000679.2:g.46768080A>G	GRCh38
NC_000017.10:g.44845446A>G , CM000679.1:g.44845446A>G	GRCh37
NG_008084.2:g.55637T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_030753.5:c.*8+232T>C (WNT3) MANE Select	NP_110380.1:n.*8+232T>C
ENST00000225512.6:c.*8+232T>C (WNT3) MANE Select	ENSP00000225512.5:n.*8+232T>C
NM_030753.4:c.*8+232T>C (WNT3)	NP_110380.1:n.*8+232T>C
ENST00000225512.5:c.*8+232T>C (WNT3)	ENSP00000225512.5:n.*8+232T>C
ENST00000706483.1:c.*8+232T>C (WNT3)	ENSP00000516407.1:n.*8+232T>C
ENST00000706484.1:c.*494+232T>C (WNT3)	ENSP00000516408.1:n.*494+232T>C
ENST00000706485.1:c.*8+232T>C (WNT3)	ENSP00000516409.1:n.*8+232T>C
ENST00000706495.1:c.*8+232T>C (WNT3)	ENSP00000516418.1:n.*8+232T>C
XM_024450773.1:c.4809+217561A>G (LRRC37A2)	XP_024306541.1:n.4809+217561A>G