Canonical Allele Identifier: CA2262378101
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773649_46773650delinsCT , CM000679.2:g.46773649_46773650delinsCT GRCh38
NC_000017.10:g.44851015_44851016delinsCT , CM000679.1:g.44851015_44851016delinsCT GRCh37
NC_000017.9:g.42206178_42206179delinsCT NCBI36
NG_008084.2:g.50067_50068delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+18_127+19delinsAG (WNT3) ENSP00000516418.1:n.127+18_127+19delinsAG...
ENST00000225512.6:c.322+18_322+19delinsAG (WNT3) MANE Select ENSP00000225512.5:n.322+18_322+19delinsAG...
ENST00000225512.5:c.322+18_322+19delinsAG (WNT3) ENSP00000225512.5:n.322+18_322+19delinsAG...
NM_030753.4:c.322+18_322+19delinsAG (WNT3) NP_110380.1:n.322+18_322+19delinsAG
XM_024450773.1:c.4809+223130_4809+223131delinsCT (LRRC37A2) XP_024306541.1:n.4809+223130_4809+223131d...
NM_030753.5:c.322+18_322+19delinsAG (WNT3) MANE Select NP_110380.1:n.322+18_322+19delinsAG
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