Canonical Allele Identifier: CA2335961188

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395495G= , CM000681.2:g.40395495G=	GRCh38
NC_000019.9:g.40901402G= , CM000681.1:g.40901402G=	GRCh37
NC_000019.8:g.45593242G=	NCBI36
NG_007979.1:g.22870C= , LRG_265:g.22870C=

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.2857C= MANE Select	NP_870998.2:p.Arg953=
ENST00000324001.8:c.2857C= MANE Select	ENSP00000326018.6:p.Arg953=
NM_020956.2:c.*3062C= , LRG_265t1:c.*3062C=	NP_066007.1:n.*3062C=
NM_181882.2:c.2857C= , LRG_265t2:c.2857C=	NP_870998.2:p.Arg953=
ENST00000291825.11:c.*3062C=	ENSP00000291825.6:n.*3062C=
ENST00000324001.7:c.2857C=	ENSP00000326018.6:p.Arg953=
ENST00000673881.1:c.2440C=	ENSP00000501070.1:p.Arg814=
ENST00000674005.2:c.3142C=	ENSP00000501261.1:p.Arg1048=
ENST00000674773.1:c.2440C=	ENSP00000502579.1:p.Arg814=
ENST00000675517.1:c.2732C=
ENST00000676076.1:c.2718C=
ENST00000676260.1:c.2819C=
ENST00000676316.1:c.2744C=
XM_011527171.1:c.2857C=	XP_011525473.1:p.Arg953=
XM_011527171.2:c.2857C=	XP_011525473.1:p.Arg953=
XM_017027046.1:c.2755C=	XP_016882535.1:p.Arg919=
XM_017027047.1:c.2755C=	XP_016882536.1:p.Arg919=