Canonical Allele Identifier: CA946986905
Gene: PRICKLE1 HGNC NCBI

Linked Data

dbSNP Id: rs1796390

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.42484802T>A , CM000674.2:g.42484802T>A GRCh38
NC_000012.11:g.42878604T>A , CM000674.1:g.42878604T>A GRCh37
NC_000012.10:g.41164871T>A NCBI36
NG_012965.1:g.109969A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000345127.9:c.-48-12238A>T MANE Select ENSP00000345064.3:n.-48-12238A>T
ENST00000445766.7:c.-48-12238A>T ENSP00000398947.2:n.-48-12238A>T
ENST00000552108.6:c.-48-12238A>T ENSP00000447870.2:n.-48-12238A>T
ENST00000639414.1:n.281-12238A>T
ENST00000639958.1:c.-45-12241A>T ENSP00000492644.1:n.-45-12241A>T
ENST00000640646.1:c.-48-12238A>T ENSP00000492483.1:n.-48-12238A>T
ENST00000640801.1:c.-48-12238A>T ENSP00000491473.1:n.-48-12238A>T
ENST00000345127.7:c.-48-12238A>T ENSP00000345064.3:n.-48-12238A>T
ENST00000445766.6:c.-48-12238A>T ENSP00000398947.2:n.-48-12238A>T
ENST00000547113.1:c.-48-12238A>T ENSP00000446699.1:n.-48-12238A>T
ENST00000552200.1:n.281-817A>T
NM_153026.2:c.-48-12238A>T NP_694571.2:n.-48-12238A>T
XM_011537947.1:c.-45-12241A>T XP_011536249.1:n.-45-12241A>T
XM_011537947.2:c.-45-12241A>T XP_011536249.1:n.-45-12241A>T
XM_017018840.1:c.-48-12238A>T XP_016874329.1:n.-48-12238A>T
NM_153026.3:c.-48-12238A>T MANE Select NP_694571.2:n.-48-12238A>T