Canonical Allele Identifier: CA150596
Gene: CTNNA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 100657
ClinVar RCV Id: RCV000087057 RCV000487676
dbSNP Id: rs587777135
MyVariant Identifiers: chr10:g.67726472_67726474del (hg19) chr10:g.65966714_65966716del (hg38)
PubMed: PMID:23136403 PMID:28699631
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.65966717_65966719del , CM000672.2:g.65966717_65966719del GRCh38
NC_000010.10:g.67726475_67726477del , CM000672.1:g.67726475_67726477del GRCh37
NC_000010.9:g.67396481_67396483del NCBI36
NG_034072.1:g.1734476_1734478del

Transcript Alleles

HGVS Amino-acid change
ENST00000373735.2:n.472_474del
ENST00000682758.1:c.2296_2298del ENSP00000508047.1:p.Leu766del
ENST00000682945.1:c.2095_2097del ENSP00000506843.1:p.Leu699del
ENST00000683624.1:c.*1835_*1837del ENSP00000507406.1:n.*1835_*1837del
ENST00000683963.1:c.*1820_*1822del ENSP00000507029.1:n.*1820_*1822del
ENST00000684154.1:c.2296_2298del ENSP00000508371.1:p.Leu766del
ENST00000433211.7:c.2296_2298del MANE Select ENSP00000389714.1:p.Leu766del
ENST00000373735.1:n.472_474del
ENST00000433211.6:c.2296_2298del ENSP00000389714.1:p.Leu766del
NM_001127384.2:c.2296_2298del NP_001120856.1:p.Leu766del
NM_013266.3:c.2296_2298del NP_037398.2:p.Leu766del
XM_005269717.2:c.2332_2334del XP_005269774.1:p.Leu778del
XM_017016151.1:c.2365_2367del XP_016871640.1:p.Leu789del
XM_017016152.1:c.2521_2523del XP_016871641.1:p.Leu841del
XM_017016153.1:c.2332_2334del XP_016871642.1:p.Leu778del
XM_017016154.1:c.1513_1515del XP_016871643.1:p.Leu505del
XM_017016155.2:c.1513_1515del XP_016871644.1:p.Leu505del
XM_017016156.1:c.1513_1515del XP_016871645.1:p.Leu505del
XM_017016157.2:c.1201_1203del XP_016871646.1:p.Leu401del
NM_013266.4:c.2296_2298del MANE Select NP_037398.2:p.Leu766del
NM_001127384.3:c.2296_2298del NP_001120856.1:p.Leu766del
Search 100 bp 5'
Search 100 bp 3'