Canonical Allele Identifier: CA405901329

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40398770G>T , CM000681.2:g.40398770G>T	GRCh38
NC_000019.9:g.40904677G>T , CM000681.1:g.40904677G>T	GRCh37
NC_000019.8:g.45596517G>T	NCBI36
NG_007979.1:g.19595C>A , LRG_265:g.19595C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.231C>A MANE Select	NP_870998.2:p.Tyr77Ter
ENST00000324001.8:c.231C>A MANE Select	ENSP00000326018.6:p.Tyr77Ter
NM_020956.2:c.231C>A , LRG_265t1:c.231C>A	NP_066007.1:p.Tyr77Ter
NM_181882.2:c.231C>A , LRG_265t2:c.231C>A	NP_870998.2:p.Tyr77Ter
ENST00000291825.11:c.231C>A	ENSP00000291825.6:p.Tyr77Ter
ENST00000324001.7:c.231C>A	ENSP00000326018.6:p.Tyr77Ter
ENST00000673881.1:c.-187C>A	ENSP00000501070.1:n.-187C>A
ENST00000674005.2:c.516C>A	ENSP00000501261.1:p.Tyr172Ter
ENST00000674642.1:n.148C>A
ENST00000674773.1:c.-36-800C>A	ENSP00000502579.1:n.-36-800C>A
ENST00000674978.1:n.278C>A
ENST00000675300.1:c.158-61C>A	ENSP00000502008.1:n.158-61C>A
ENST00000675517.1:c.47C>A
ENST00000676076.1:c.47C>A
ENST00000676260.1:c.47C>A
ENST00000676316.1:c.47C>A
XM_011527171.1:c.231C>A	XP_011525473.1:p.Tyr77Ter
XM_011527171.2:c.231C>A	XP_011525473.1:p.Tyr77Ter
XM_017027046.1:c.129C>A	XP_016882535.1:p.Tyr43Ter
XM_017027047.1:c.129C>A	XP_016882536.1:p.Tyr43Ter