Canonical Allele Identifier: CA2479768
Gene: PRICKLE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 346476
dbSNP Id: rs144338942
gnomAD v2: 3-64138955-G-A
gnomAD v3: 3-64153279-G-A
gnomAD v4: 3-64153279-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.64153279G>A , CM000665.2:g.64153279G>A GRCh38
NC_000003.11:g.64138955G>A , CM000665.1:g.64138955G>A GRCh37
NC_000003.10:g.64113995G>A NCBI36
NG_031930.1:g.77177C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295902.11:c.858C>T ENSP00000295902.7:p.Gly286=
ENST00000564377.6:c.690C>T ENSP00000455004.2:p.Gly230=
ENST00000638394.2:c.690C>T MANE Select ENSP00000492363.1:p.Gly230=
ENST00000640095.1:n.1758C>T
ENST00000640303.1:n.1329C>T
ENST00000295902.10:c.690C>T ENSP00000295902.6:p.Gly230=
ENST00000564377.5:c.858C>T ENSP00000455004.1:p.Gly286=
NM_198859.3:c.690C>T NP_942559.1:p.Gly230=
XM_011533432.1:c.966C>T XP_011531734.1:p.Gly322=
XM_011533433.1:c.966C>T XP_011531735.1:p.Gly322=
XM_011533434.1:c.858C>T XP_011531736.1:p.Gly286=
XM_011533435.1:c.858C>T XP_011531737.1:p.Gly286=
XM_011533436.1:c.690C>T XP_011531738.1:p.Gly230=
XM_011533437.1:c.690C>T XP_011531739.1:p.Gly230=
XM_011533438.1:c.339C>T XP_011531740.1:p.Gly113=
XM_011533439.1:c.690C>T XP_011531741.1:p.Gly230=
XM_011533440.1:c.966C>T XP_011531742.1:p.Gly322=
XM_011533432.2:c.966C>T XP_011531734.1:p.Gly322=
XM_011533433.2:c.966C>T XP_011531735.1:p.Gly322=
XM_011533434.2:c.858C>T XP_011531736.1:p.Gly286=
XM_011533435.2:c.858C>T XP_011531737.1:p.Gly286=
XM_011533436.3:c.690C>T XP_011531738.1:p.Gly230=
XM_011533437.2:c.690C>T XP_011531739.1:p.Gly230=
XM_011533438.2:c.339C>T XP_011531740.1:p.Gly113=
XM_011533440.2:c.966C>T XP_011531742.1:p.Gly322=
XM_017005798.1:c.690C>T XP_016861287.1:p.Gly230=
XM_017005799.1:c.318C>T XP_016861288.1:p.Gly106=
NM_198859.4:c.690C>T MANE Select NP_942559.1:p.Gly230=
NM_001370528.1:c.690C>T NP_001357457.1:p.Gly230=