Canonical Allele Identifier: CA2335961435

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396057G= , CM000681.2:g.40396057G=	GRCh38
NC_000019.9:g.40901964G= , CM000681.1:g.40901964G=	GRCh37
NC_000019.8:g.45593804G=	NCBI36
NG_007979.1:g.22308C= , LRG_265:g.22308C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2295C= MANE Select	ENSP00000326018.6:p.Asp765=
ENST00000673881.1:c.1878C=	ENSP00000501070.1:p.Asp626=
ENST00000674005.2:c.2580C=	ENSP00000501261.1:p.Asp860=
ENST00000674773.1:c.1878C=	ENSP00000502579.1:p.Asp626=
ENST00000675517.1:c.2170C=
ENST00000676076.1:c.2156C=
ENST00000676260.1:c.2257C=
ENST00000676316.1:c.2182C=
ENST00000291825.11:c.*2500C=	ENSP00000291825.6:n.*2500C=
ENST00000324001.7:c.2295C=	ENSP00000326018.6:p.Asp765=
NM_020956.2:c.*2500C= , LRG_265t1:c.*2500C=	NP_066007.1:n.*2500C=
NM_181882.2:c.2295C= , LRG_265t2:c.2295C=	NP_870998.2:p.Asp765=
XM_011527171.1:c.2295C=	XP_011525473.1:p.Asp765=
XM_011527171.2:c.2295C=	XP_011525473.1:p.Asp765=
XM_017027046.1:c.2193C=	XP_016882535.1:p.Asp731=
XM_017027047.1:c.2193C=	XP_016882536.1:p.Asp731=
NM_181882.3:c.2295C= MANE Select	NP_870998.2:p.Asp765=