Canonical Allele Identifier: CA9444389

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40397625C>T , CM000681.2:g.40397625C>T	GRCh38
NC_000019.9:g.40903532C>T , CM000681.1:g.40903532C>T	GRCh37
NC_000019.8:g.45595372C>T	NCBI36
NG_007979.1:g.20740G>A , LRG_265:g.20740G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.727G>A MANE Select	NP_870998.2:p.Gly243Arg
ENST00000324001.8:c.727G>A MANE Select	ENSP00000326018.6:p.Gly243Arg
NM_020956.2:c.*932G>A , LRG_265t1:c.*932G>A	NP_066007.1:n.*932G>A
NM_181882.2:c.727G>A , LRG_265t2:c.727G>A	NP_870998.2:p.Gly243Arg
ENST00000291825.11:c.*932G>A	ENSP00000291825.6:n.*932G>A
ENST00000324001.7:c.727G>A	ENSP00000326018.6:p.Gly243Arg
ENST00000673881.1:c.310G>A	ENSP00000501070.1:p.Gly104Arg
ENST00000674005.2:c.1012G>A	ENSP00000501261.1:p.Gly338Arg
ENST00000674773.1:c.310G>A	ENSP00000502579.1:p.Gly104Arg
ENST00000675517.1:c.602G>A
ENST00000676076.1:c.588G>A
ENST00000676260.1:c.689G>A
ENST00000676316.1:c.614G>A
XM_011527171.1:c.727G>A	XP_011525473.1:p.Gly243Arg
XM_011527171.2:c.727G>A	XP_011525473.1:p.Gly243Arg
XM_017027046.1:c.625G>A	XP_016882535.1:p.Gly209Arg
XM_017027047.1:c.625G>A	XP_016882536.1:p.Gly209Arg