Canonical Allele Identifier: CA405901390

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40398796G>A , CM000681.2:g.40398796G>A	GRCh38
NC_000019.9:g.40904703G>A , CM000681.1:g.40904703G>A	GRCh37
NC_000019.8:g.45596543G>A	NCBI36
NG_007979.1:g.19569C>T , LRG_265:g.19569C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.205C>T MANE Select	NP_870998.2:p.Arg69Ter
ENST00000324001.8:c.205C>T MANE Select	ENSP00000326018.6:p.Arg69Ter
NM_020956.2:c.205C>T , LRG_265t1:c.205C>T	NP_066007.1:p.Arg69Ter
NM_181882.2:c.205C>T , LRG_265t2:c.205C>T	NP_870998.2:p.Arg69Ter
ENST00000291825.11:c.205C>T	ENSP00000291825.6:p.Arg69Ter
ENST00000324001.7:c.205C>T	ENSP00000326018.6:p.Arg69Ter
ENST00000673881.1:c.-213C>T	ENSP00000501070.1:n.-213C>T
ENST00000674005.2:c.490C>T	ENSP00000501261.1:p.Arg164Ter
ENST00000674642.1:n.122C>T
ENST00000674773.1:c.-36-826C>T	ENSP00000502579.1:n.-36-826C>T
ENST00000674978.1:n.252C>T
ENST00000675300.1:c.158-87C>T	ENSP00000502008.1:n.158-87C>T
ENST00000675517.1:c.21C>T
ENST00000676076.1:c.21C>T
ENST00000676260.1:c.21C>T
ENST00000676316.1:c.21C>T
XM_011527171.1:c.205C>T	XP_011525473.1:p.Arg69Ter
XM_011527171.2:c.205C>T	XP_011525473.1:p.Arg69Ter
XM_017027046.1:c.103C>T	XP_016882535.1:p.Arg35Ter
XM_017027047.1:c.103C>T	XP_016882536.1:p.Arg35Ter