Canonical Allele Identifier: CA9444001

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395663G>A , CM000681.2:g.40395663G>A	GRCh38
NC_000019.9:g.40901570G>A , CM000681.1:g.40901570G>A	GRCh37
NC_000019.8:g.45593410G>A	NCBI36
NG_007979.1:g.22702C>T , LRG_265:g.22702C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.2689C>T MANE Select	NP_870998.2:p.Arg897Ter
ENST00000324001.8:c.2689C>T MANE Select	ENSP00000326018.6:p.Arg897Ter
NM_020956.2:c.*2894C>T , LRG_265t1:c.*2894C>T	NP_066007.1:n.*2894C>T
NM_181882.2:c.2689C>T , LRG_265t2:c.2689C>T	NP_870998.2:p.Arg897Ter
ENST00000291825.11:c.*2894C>T	ENSP00000291825.6:n.*2894C>T
ENST00000324001.7:c.2689C>T	ENSP00000326018.6:p.Arg897Ter
ENST00000673881.1:c.2272C>T	ENSP00000501070.1:p.Arg758Ter
ENST00000674005.2:c.2974C>T	ENSP00000501261.1:p.Arg992Ter
ENST00000674773.1:c.2272C>T	ENSP00000502579.1:p.Arg758Ter
ENST00000675517.1:c.2564C>T
ENST00000676076.1:c.2550C>T
ENST00000676260.1:c.2651C>T
ENST00000676316.1:c.2576C>T
XM_011527171.1:c.2689C>T	XP_011525473.1:p.Arg897Ter
XM_011527171.2:c.2689C>T	XP_011525473.1:p.Arg897Ter
XM_017027046.1:c.2587C>T	XP_016882535.1:p.Arg863Ter
XM_017027047.1:c.2587C>T	XP_016882536.1:p.Arg863Ter