Canonical Allele Identifier: CA2335961500

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396164G= , CM000681.2:g.40396164G=	GRCh38
NC_000019.9:g.40902071G= , CM000681.1:g.40902071G=	GRCh37
NC_000019.8:g.45593911G=	NCBI36
NG_007979.1:g.22201C= , LRG_265:g.22201C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2188C= MANE Select	ENSP00000326018.6:p.Pro730=
ENST00000673881.1:c.1771C=	ENSP00000501070.1:p.Pro591=
ENST00000674005.2:c.2473C=	ENSP00000501261.1:p.Pro825=
ENST00000674773.1:c.1771C=	ENSP00000502579.1:p.Pro591=
ENST00000675517.1:c.2063C=
ENST00000676076.1:c.2049C=
ENST00000676260.1:c.2150C=
ENST00000676316.1:c.2075C=
ENST00000291825.11:c.*2393C=	ENSP00000291825.6:n.*2393C=
ENST00000324001.7:c.2188C=	ENSP00000326018.6:p.Pro730=
NM_020956.2:c.*2393C= , LRG_265t1:c.*2393C=	NP_066007.1:n.*2393C=
NM_181882.2:c.2188C= , LRG_265t2:c.2188C=	NP_870998.2:p.Pro730=
XM_011527171.1:c.2188C=	XP_011525473.1:p.Pro730=
XM_011527171.2:c.2188C=	XP_011525473.1:p.Pro730=
XM_017027046.1:c.2086C=	XP_016882535.1:p.Pro696=
XM_017027047.1:c.2086C=	XP_016882536.1:p.Pro696=
NM_181882.3:c.2188C= MANE Select	NP_870998.2:p.Pro730=