Canonical Allele Identifier: CA2262378236
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773987_46773993delinsACCCTCC , CM000679.2:g.46773987_46773993delinsACCCTCC GRCh38
NC_000017.10:g.44851353_44851359delinsACCCTCC , CM000679.1:g.44851353_44851359delinsACCCTCC GRCh37
NC_000017.9:g.42206516_42206522delinsACCCTCC NCBI36
NG_008084.2:g.49724_49730delinsGGAGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-115-84_-115-78delinsGGAGGGT (WNT3) ENSP00000516418.1:n.-115-84_-115-78delinsGGAGGGT
ENST00000225512.6:c.81-84_81-78delinsGGAGGGT (WNT3) MANE Select ENSP00000225512.5:n.81-84_81-78delinsGGAGGGT
ENST00000225512.5:c.81-84_81-78delinsGGAGGGT (WNT3) ENSP00000225512.5:n.81-84_81-78delinsGGAGGGT
ENST00000573788.5:n.492-84_492-78delinsGGAGGGT (WNT3)
NM_030753.4:c.81-84_81-78delinsGGAGGGT (WNT3) NP_110380.1:n.81-84_81-78delinsGGAGGGT
XM_024450773.1:c.4809+223468_4809+223474delinsACCCTCC (LRRC37A2) XP_024306541.1:n.4809+223468_4809+223474delinsACCCTCC
NM_030753.5:c.81-84_81-78delinsGGAGGGT (WNT3) MANE Select NP_110380.1:n.81-84_81-78delinsGGAGGGT