Canonical Allele Identifier: CA76161345
Gene: PRICKLE2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.64306961A>T , CM000665.2:g.64306961A>T GRCh38
NC_000003.11:g.64292637A>T , CM000665.1:g.64292637A>T GRCh37
NC_000003.10:g.64267677A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295902.11:c.129-107994T>A ENSP00000295902.7:n.129-107994T>A
ENST00000485770.2:n.341-107994T>A
ENST00000498162.2:c.110-107994T>A
ENST00000564377.5:c.129-107994T>A ENSP00000455004.1:n.129-107994T>A
ENST00000569824.1:c.237-107994T>A ENSP00000456173.1:n.237-107994T>A
XM_011533432.1:c.237-107994T>A XP_011531734.1:n.237-107994T>A
XM_011533433.1:c.237-107994T>A XP_011531735.1:n.237-107994T>A
XM_011533434.1:c.129-107994T>A XP_011531736.1:n.129-107994T>A
XM_011533435.1:c.129-107994T>A XP_011531737.1:n.129-107994T>A
XM_011533440.1:c.237-107994T>A XP_011531742.1:n.237-107994T>A
XM_011533432.2:c.237-107994T>A XP_011531734.1:n.237-107994T>A
XM_011533433.2:c.237-107994T>A XP_011531735.1:n.237-107994T>A
XM_011533434.2:c.129-107994T>A XP_011531736.1:n.129-107994T>A
XM_011533435.2:c.129-107994T>A XP_011531737.1:n.129-107994T>A
XM_011533440.2:c.237-107994T>A XP_011531742.1:n.237-107994T>A
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