Canonical Allele Identifier: CA1370523115

Gene: PRICKLE2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.64157319C= , CM000665.2:g.64157319C=	GRCh38
NC_000003.11:g.64142995C= , CM000665.1:g.64142995C=	GRCh37
NC_000003.10:g.64118035C=	NCBI36
NG_031930.1:g.73137G=

Transcript Alleles

HGVS	Amino-acid Change
NM_198859.4:c.443G= MANE Select	NP_942559.1:p.Arg148=
ENST00000638394.2:c.443G= MANE Select	ENSP00000492363.1:p.Arg148=
NM_001370528.1:c.443G=	NP_001357457.1:p.Arg148=
NM_198859.3:c.443G=	NP_942559.1:p.Arg148=
ENST00000295902.10:c.443G=	ENSP00000295902.6:p.Arg148=
ENST00000295902.11:c.611G=	ENSP00000295902.7:p.Arg204=
ENST00000498162.1:c.443G=	ENSP00000419951.1:p.Arg148=
ENST00000564377.5:c.611G=	ENSP00000455004.1:p.Arg204=
ENST00000564377.6:c.443G=	ENSP00000455004.2:p.Arg148=
ENST00000640303.1:n.1082G=
XM_011533432.1:c.719G=	XP_011531734.1:p.Arg240=
XM_011533432.2:c.719G=	XP_011531734.1:p.Arg240=
XM_011533433.1:c.719G=	XP_011531735.1:p.Arg240=
XM_011533433.2:c.719G=	XP_011531735.1:p.Arg240=
XM_011533434.1:c.611G=	XP_011531736.1:p.Arg204=
XM_011533434.2:c.611G=	XP_011531736.1:p.Arg204=
XM_011533435.1:c.611G=	XP_011531737.1:p.Arg204=
XM_011533435.2:c.611G=	XP_011531737.1:p.Arg204=
XM_011533436.1:c.443G=	XP_011531738.1:p.Arg148=
XM_011533436.3:c.443G=	XP_011531738.1:p.Arg148=
XM_011533437.1:c.443G=	XP_011531739.1:p.Arg148=
XM_011533437.2:c.443G=	XP_011531739.1:p.Arg148=
XM_011533438.1:c.92G=	XP_011531740.1:p.Arg31=
XM_011533438.2:c.92G=	XP_011531740.1:p.Arg31=
XM_011533439.1:c.443G=	XP_011531741.1:p.Arg148=
XM_011533440.1:c.719G=	XP_011531742.1:p.Arg240=
XM_011533440.2:c.719G=	XP_011531742.1:p.Arg240=
XM_017005798.1:c.443G=	XP_016861287.1:p.Arg148=
XM_017005799.1:c.71G=	XP_016861288.1:p.Arg24=