Canonical Allele Identifier: CA9443679

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394200C>T , CM000681.2:g.40394200C>T	GRCh38
NC_000019.9:g.40900107C>T , CM000681.1:g.40900107C>T	GRCh37
NC_000019.8:g.45591947C>T	NCBI36
NG_007979.1:g.24165G>A , LRG_265:g.24165G>A
NG_051224.1:g.1022G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.4152G>A MANE Select	ENSP00000326018.6:p.Ala1384=
ENST00000673881.1:c.3735G>A	ENSP00000501070.1:p.Ala1245=
ENST00000674005.2:c.4437G>A	ENSP00000501261.1:p.Ala1479=
ENST00000674773.1:c.3735G>A	ENSP00000502579.1:p.Ala1245=
ENST00000675517.1:c.4027G>A
ENST00000676076.1:c.4013G>A
ENST00000676260.1:c.4114G>A
ENST00000676316.1:c.4039G>A
ENST00000291825.11:c.*4357G>A	ENSP00000291825.6:n.*4357G>A
ENST00000324001.7:c.4152G>A	ENSP00000326018.6:p.Ala1384=
NM_020956.2:c.*4357G>A , LRG_265t1:c.*4357G>A	NP_066007.1:n.*4357G>A
NM_181882.2:c.4152G>A , LRG_265t2:c.4152G>A	NP_870998.2:p.Ala1384=
XM_011527171.1:c.4152G>A	XP_011525473.1:p.Ala1384=
XM_011527171.2:c.4152G>A	XP_011525473.1:p.Ala1384=
XM_017027046.1:c.4050G>A	XP_016882535.1:p.Ala1350=
XM_017027047.1:c.4050G>A	XP_016882536.1:p.Ala1350=
NM_181882.3:c.4152G>A MANE Select	NP_870998.2:p.Ala1384=