Canonical Allele Identifier: CA2335962032

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40397178G= , CM000681.2:g.40397178G=	GRCh38
NC_000019.9:g.40903085G= , CM000681.1:g.40903085G=	GRCh37
NC_000019.8:g.45594925G=	NCBI36
NG_007979.1:g.21187C= , LRG_265:g.21187C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.1174C= MANE Select	ENSP00000326018.6:p.Arg392=
ENST00000673881.1:c.757C=	ENSP00000501070.1:p.Arg253=
ENST00000674005.2:c.1459C=	ENSP00000501261.1:p.Arg487=
ENST00000674773.1:c.757C=	ENSP00000502579.1:p.Arg253=
ENST00000675517.1:c.1049C=
ENST00000676076.1:c.1035C=
ENST00000676260.1:c.1136C=
ENST00000676316.1:c.1061C=
ENST00000291825.11:c.*1379C=	ENSP00000291825.6:n.*1379C=
ENST00000324001.7:c.1174C=	ENSP00000326018.6:p.Arg392=
NM_020956.2:c.*1379C= , LRG_265t1:c.*1379C=	NP_066007.1:n.*1379C=
NM_181882.2:c.1174C= , LRG_265t2:c.1174C=	NP_870998.2:p.Arg392=
XM_011527171.1:c.1174C=	XP_011525473.1:p.Arg392=
XM_011527171.2:c.1174C=	XP_011525473.1:p.Arg392=
XM_017027046.1:c.1072C=	XP_016882535.1:p.Arg358=
XM_017027047.1:c.1072C=	XP_016882536.1:p.Arg358=
NM_181882.3:c.1174C= MANE Select	NP_870998.2:p.Arg392=