Canonical Allele Identifier: CA2479653

Gene: PRICKLE2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.64147173G>A , CM000665.2:g.64147173G>A	GRCh38
NC_000003.11:g.64132849G>A , CM000665.1:g.64132849G>A	GRCh37
NC_000003.10:g.64107889G>A	NCBI36
NG_031930.1:g.83283C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295902.11:c.1485C>T	ENSP00000295902.7:p.Pro495=
ENST00000564377.6:c.1317C>T	ENSP00000455004.2:p.Pro439=
ENST00000638394.2:c.1317C>T MANE Select	ENSP00000492363.1:p.Pro439=
ENST00000640095.1:n.2385C>T
ENST00000640303.1:n.1956C>T
ENST00000295902.10:c.1317C>T	ENSP00000295902.6:p.Pro439=
ENST00000564377.5:c.1485C>T	ENSP00000455004.1:p.Pro495=
NM_198859.3:c.1317C>T	NP_942559.1:p.Pro439=
XM_011533432.1:c.1593C>T	XP_011531734.1:p.Pro531=
XM_011533433.1:c.1593C>T	XP_011531735.1:p.Pro531=
XM_011533434.1:c.1485C>T	XP_011531736.1:p.Pro495=
XM_011533435.1:c.1485C>T	XP_011531737.1:p.Pro495=
XM_011533436.1:c.1317C>T	XP_011531738.1:p.Pro439=
XM_011533437.1:c.1317C>T	XP_011531739.1:p.Pro439=
XM_011533438.1:c.966C>T	XP_011531740.1:p.Pro322=
XM_011533439.1:c.1317C>T	XP_011531741.1:p.Pro439=
XM_011533440.1:c.1593C>T	XP_011531742.1:p.Pro531=
XM_011533432.2:c.1593C>T	XP_011531734.1:p.Pro531=
XM_011533433.2:c.1593C>T	XP_011531735.1:p.Pro531=
XM_011533434.2:c.1485C>T	XP_011531736.1:p.Pro495=
XM_011533435.2:c.1485C>T	XP_011531737.1:p.Pro495=
XM_011533436.3:c.1317C>T	XP_011531738.1:p.Pro439=
XM_011533437.2:c.1317C>T	XP_011531739.1:p.Pro439=
XM_011533438.2:c.966C>T	XP_011531740.1:p.Pro322=
XM_011533440.2:c.1593C>T	XP_011531742.1:p.Pro531=
XM_017005798.1:c.1317C>T	XP_016861287.1:p.Pro439=
XM_017005799.1:c.945C>T	XP_016861288.1:p.Pro315=
NM_198859.4:c.1317C>T MANE Select	NP_942559.1:p.Pro439=
NM_001370528.1:c.1317C>T	NP_001357457.1:p.Pro439=