Canonical Allele Identifier: CA2031934116
Gene: PRICKLE1 HGNC NCBI

Linked Data

dbSNP Id: rs1796390

Genomic Alleles

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

Transcript Alleles

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