Canonical Allele Identifier: CA9444424

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40397766G>T , CM000681.2:g.40397766G>T	GRCh38
NC_000019.9:g.40903673G>T , CM000681.1:g.40903673G>T	GRCh37
NC_000019.8:g.45595513G>T	NCBI36
NG_007979.1:g.20599C>A , LRG_265:g.20599C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.586C>A MANE Select	NP_870998.2:p.Arg196=
ENST00000324001.8:c.586C>A MANE Select	ENSP00000326018.6:p.Arg196=
NM_020956.2:c.*791C>A , LRG_265t1:c.*791C>A	NP_066007.1:n.*791C>A
NM_181882.2:c.586C>A , LRG_265t2:c.586C>A	NP_870998.2:p.Arg196=
ENST00000291825.11:c.*791C>A	ENSP00000291825.6:n.*791C>A
ENST00000324001.7:c.586C>A	ENSP00000326018.6:p.Arg196=
ENST00000673881.1:c.169C>A	ENSP00000501070.1:p.Arg57=
ENST00000674005.2:c.871C>A	ENSP00000501261.1:p.Arg291=
ENST00000674773.1:c.169C>A	ENSP00000502579.1:p.Arg57=
ENST00000675517.1:c.461C>A
ENST00000676076.1:c.447C>A
ENST00000676260.1:c.548C>A
ENST00000676316.1:c.473C>A
XM_011527171.1:c.586C>A	XP_011525473.1:p.Arg196=
XM_011527171.2:c.586C>A	XP_011525473.1:p.Arg196=
XM_017027046.1:c.484C>A	XP_016882535.1:p.Arg162=
XM_017027047.1:c.484C>A	XP_016882536.1:p.Arg162=