Canonical Allele Identifier: CA2618361803
Gene: PRICKLE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.42469371_42469372del , CM000674.2:g.42469371_42469372del GRCh38
NC_000012.11:g.42863173_42863174del , CM000674.1:g.42863173_42863174del GRCh37
NC_000012.10:g.41149440_41149441del NCBI36
NG_012965.1:g.125399_125400del

Transcript Alleles

HGVS Amino-acid change
ENST00000345127.9:c.384+78_384+79del MANE Select ENSP00000345064.3:n.384+78_384+79del
ENST00000445766.7:c.384+78_384+79del ENSP00000398947.2:n.384+78_384+79del
ENST00000455697.6:c.384+78_384+79del ENSP00000401060.1:n.384+78_384+79del
ENST00000548696.6:c.384+78_384+79del ENSP00000448359.1:n.384+78_384+79del
ENST00000552108.6:c.384+78_384+79del ENSP00000447870.2:n.384+78_384+79del
ENST00000552240.6:c.384+78_384+79del ENSP00000449819.1:n.384+78_384+79del
ENST00000639566.1:c.384+78_384+79del ENSP00000492332.1:n.384+78_384+79del
ENST00000639589.1:c.384+78_384+79del ENSP00000491051.1:n.384+78_384+79del
ENST00000639958.1:c.384+78_384+79del ENSP00000492644.1:n.384+78_384+79del
ENST00000640055.1:c.384+78_384+79del ENSP00000492763.1:n.384+78_384+79del
ENST00000640132.1:c.384+78_384+79del ENSP00000491228.1:n.384+78_384+79del
ENST00000640840.1:n.211+78_211+79del
ENST00000345127.7:c.384+78_384+79del ENSP00000345064.3:n.384+78_384+79del
ENST00000445766.6:c.384+78_384+79del ENSP00000398947.2:n.384+78_384+79del
ENST00000455697.5:c.384+78_384+79del ENSP00000401060.1:n.384+78_384+79del
ENST00000548696.5:c.384+78_384+79del ENSP00000448359.1:n.384+78_384+79del
ENST00000552108.5:c.384+78_384+79del ENSP00000447870.1:n.384+78_384+79del
ENST00000552240.5:c.384+78_384+79del ENSP00000449819.1:n.384+78_384+79del
NM_001144881.1:c.384+78_384+79del NP_001138353.1:n.384+78_384+79del
NM_001144882.1:c.384+78_384+79del NP_001138354.1:n.384+78_384+79del
NM_001144883.1:c.384+78_384+79del NP_001138355.1:n.384+78_384+79del
NM_153026.2:c.384+78_384+79del NP_694571.2:n.384+78_384+79del
XM_011537946.1:c.384+78_384+79del XP_011536248.1:n.384+78_384+79del
XM_011537947.1:c.384+78_384+79del XP_011536249.1:n.384+78_384+79del
XM_011537947.2:c.384+78_384+79del XP_011536249.1:n.384+78_384+79del
XM_017018838.1:c.384+78_384+79del XP_016874327.1:n.384+78_384+79del
XM_017018839.1:c.384+78_384+79del XP_016874328.1:n.384+78_384+79del
XM_017018840.1:c.384+78_384+79del XP_016874329.1:n.384+78_384+79del
NM_153026.3:c.384+78_384+79del MANE Select NP_694571.2:n.384+78_384+79del
NM_001144881.2:c.384+78_384+79del NP_001138353.1:n.384+78_384+79del
NM_001144882.2:c.384+78_384+79del NP_001138354.1:n.384+78_384+79del
NM_001144883.2:c.384+78_384+79del NP_001138355.1:n.384+78_384+79del