Canonical Allele Identifier: CA8620617
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs767598317
ExAC: 17:44850985 TCCCTCCCCCCACCCAGC / T
gnomAD v2: 17-44850985-TCCCTCCCCCCACCCAGC-T
gnomAD v3: 17-46773619-TCCCTCCCCCCACCCAGC-T
gnomAD v4: 17-46773619-TCCCTCCCCCCACCCAGC-T
MyVariant Identifiers: chr17:g.44850986_44851002del (hg19) chr17:g.46773620_46773636del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773630_46773646del , CM000679.2:g.46773630_46773646del GRCh38
NC_000017.10:g.44850996_44851012del , CM000679.1:g.44850996_44851012del GRCh37
NC_000017.9:g.42206159_42206175del NCBI36
NG_008084.2:g.50081_50097del

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+32_127+48del (WNT3) ENSP00000516418.1:n.127+32_127+48del
ENST00000225512.6:c.322+32_322+48del (WNT3) MANE Select ENSP00000225512.5:n.322+32_322+48del
ENST00000225512.5:c.322+32_322+48del (WNT3) ENSP00000225512.5:n.322+32_322+48del
NM_030753.4:c.322+32_322+48del (WNT3) NP_110380.1:n.322+32_322+48del
XM_024450773.1:c.4809+223111_4809+223127del (LRRC37A2) XP_024306541.1:n.4809+223111_4809+223127d...
NM_030753.5:c.322+32_322+48del (WNT3) MANE Select NP_110380.1:n.322+32_322+48del
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