Canonical Allele Identifier: CA2335961422

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396032C= , CM000681.2:g.40396032C=	GRCh38
NC_000019.9:g.40901939C= , CM000681.1:g.40901939C=	GRCh37
NC_000019.8:g.45593779C=	NCBI36
NG_007979.1:g.22333G= , LRG_265:g.22333G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2320G= MANE Select	ENSP00000326018.6:p.Val774=
ENST00000673881.1:c.1903G=	ENSP00000501070.1:p.Val635=
ENST00000674005.2:c.2605G=	ENSP00000501261.1:p.Val869=
ENST00000674773.1:c.1903G=	ENSP00000502579.1:p.Val635=
ENST00000675517.1:c.2195G=
ENST00000676076.1:c.2181G=
ENST00000676260.1:c.2282G=
ENST00000676316.1:c.2207G=
ENST00000291825.11:c.*2525G=	ENSP00000291825.6:n.*2525G=
ENST00000324001.7:c.2320G=	ENSP00000326018.6:p.Val774=
NM_020956.2:c.*2525G= , LRG_265t1:c.*2525G=	NP_066007.1:n.*2525G=
NM_181882.2:c.2320G= , LRG_265t2:c.2320G=	NP_870998.2:p.Val774=
XM_011527171.1:c.2320G=	XP_011525473.1:p.Val774=
XM_011527171.2:c.2320G=	XP_011525473.1:p.Val774=
XM_017027046.1:c.2218G=	XP_016882535.1:p.Val740=
XM_017027047.1:c.2218G=	XP_016882536.1:p.Val740=
NM_181882.3:c.2320G= MANE Select	NP_870998.2:p.Val774=