Canonical Allele Identifier: CA2335961407

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395984C= , CM000681.2:g.40395984C=	GRCh38
NC_000019.9:g.40901891C= , CM000681.1:g.40901891C=	GRCh37
NC_000019.8:g.45593731C=	NCBI36
NG_007979.1:g.22381G= , LRG_265:g.22381G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2368G= MANE Select	ENSP00000326018.6:p.Glu790=
ENST00000673881.1:c.1951G=	ENSP00000501070.1:p.Glu651=
ENST00000674005.2:c.2653G=	ENSP00000501261.1:p.Glu885=
ENST00000674773.1:c.1951G=	ENSP00000502579.1:p.Glu651=
ENST00000675517.1:c.2243G=
ENST00000676076.1:c.2229G=
ENST00000676260.1:c.2330G=
ENST00000676316.1:c.2255G=
ENST00000291825.11:c.*2573G=	ENSP00000291825.6:n.*2573G=
ENST00000324001.7:c.2368G=	ENSP00000326018.6:p.Glu790=
NM_020956.2:c.*2573G= , LRG_265t1:c.*2573G=	NP_066007.1:n.*2573G=
NM_181882.2:c.2368G= , LRG_265t2:c.2368G=	NP_870998.2:p.Glu790=
XM_011527171.1:c.2368G=	XP_011525473.1:p.Glu790=
XM_011527171.2:c.2368G=	XP_011525473.1:p.Glu790=
XM_017027046.1:c.2266G=	XP_016882535.1:p.Glu756=
XM_017027047.1:c.2266G=	XP_016882536.1:p.Glu756=
NM_181882.3:c.2368G= MANE Select	NP_870998.2:p.Glu790=