Canonical Allele Identifier: CA384444274

Gene: PRICKLE1

Linked Data

• MyVariant Identifiers: chr12:g.42863332C>A (hg19) ; chr12:g.42469530C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.42469530C>A , CM000674.2:g.42469530C>A	GRCh38
NC_000012.11:g.42863332C>A , CM000674.1:g.42863332C>A	GRCh37
NC_000012.10:g.41149599C>A	NCBI36
NG_012965.1:g.125241G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345127.9:c.304G>T MANE Select	ENSP00000345064.3:p.Ala102Ser
ENST00000445766.7:c.304G>T	ENSP00000398947.2:p.Ala102Ser
ENST00000455697.6:c.304G>T	ENSP00000401060.1:p.Ala102Ser
ENST00000548696.6:c.304G>T	ENSP00000448359.1:p.Ala102Ser
ENST00000551050.6:c.304G>T	ENSP00000446970.1:p.Ala102Ser
ENST00000552108.6:c.304G>T	ENSP00000447870.2:p.Ala102Ser
ENST00000552240.6:c.304G>T	ENSP00000449819.1:p.Ala102Ser
ENST00000639566.1:c.304G>T	ENSP00000492332.1:p.Ala102Ser
ENST00000639589.1:c.304G>T	ENSP00000491051.1:p.Ala102Ser
ENST00000639958.1:c.304G>T	ENSP00000492644.1:p.Ala102Ser
ENST00000640055.1:c.304G>T	ENSP00000492763.1:p.Ala102Ser
ENST00000640132.1:c.304G>T	ENSP00000491228.1:p.Ala102Ser
ENST00000640646.1:c.304G>T	ENSP00000492483.1:p.Ala102Ser
ENST00000640801.1:c.304G>T	ENSP00000491473.1:p.Ala102Ser
ENST00000640840.1:n.131G>T
ENST00000345127.7:c.304G>T	ENSP00000345064.3:p.Ala102Ser
ENST00000445766.6:c.304G>T	ENSP00000398947.2:p.Ala102Ser
ENST00000455697.5:c.304G>T	ENSP00000401060.1:p.Ala102Ser
ENST00000547113.1:c.304G>T	ENSP00000446699.1:p.Ala102Ser
ENST00000548696.5:c.304G>T	ENSP00000448359.1:p.Ala102Ser
ENST00000551050.5:c.304G>T	ENSP00000446970.1:p.Ala102Ser
ENST00000552108.5:c.304G>T	ENSP00000447870.1:p.Ala102Ser
ENST00000552240.5:c.304G>T	ENSP00000449819.1:p.Ala102Ser
NM_001144881.1:c.304G>T	NP_001138353.1:p.Ala102Ser
NM_001144882.1:c.304G>T	NP_001138354.1:p.Ala102Ser
NM_001144883.1:c.304G>T	NP_001138355.1:p.Ala102Ser
NM_153026.2:c.304G>T	NP_694571.2:p.Ala102Ser
XM_011537946.1:c.304G>T	XP_011536248.1:p.Ala102Ser
XM_011537947.1:c.304G>T	XP_011536249.1:p.Ala102Ser
XM_011537947.2:c.304G>T	XP_011536249.1:p.Ala102Ser
XM_017018838.1:c.304G>T	XP_016874327.1:p.Ala102Ser
XM_017018839.1:c.304G>T	XP_016874328.1:p.Ala102Ser
XM_017018840.1:c.304G>T	XP_016874329.1:p.Ala102Ser
NM_153026.3:c.304G>T MANE Select	NP_694571.2:p.Ala102Ser
NM_001144881.2:c.304G>T	NP_001138353.1:p.Ala102Ser
NM_001144882.2:c.304G>T	NP_001138354.1:p.Ala102Ser
NM_001144883.2:c.304G>T	NP_001138355.1:p.Ala102Ser