Canonical Allele Identifier: CA405897010

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396254C>T , CM000681.2:g.40396254C>T	GRCh38
NC_000019.9:g.40902161C>T , CM000681.1:g.40902161C>T	GRCh37
NC_000019.8:g.45594001C>T	NCBI36
NG_007979.1:g.22111G>A , LRG_265:g.22111G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.2098G>A MANE Select	NP_870998.2:p.Ala700Thr
ENST00000324001.8:c.2098G>A MANE Select	ENSP00000326018.6:p.Ala700Thr
NM_020956.2:c.*2303G>A , LRG_265t1:c.*2303G>A	NP_066007.1:n.*2303G>A
NM_181882.2:c.2098G>A , LRG_265t2:c.2098G>A	NP_870998.2:p.Ala700Thr
ENST00000291825.11:c.*2303G>A	ENSP00000291825.6:n.*2303G>A
ENST00000324001.7:c.2098G>A	ENSP00000326018.6:p.Ala700Thr
ENST00000673881.1:c.1681G>A	ENSP00000501070.1:p.Ala561Thr
ENST00000674005.2:c.2383G>A	ENSP00000501261.1:p.Ala795Thr
ENST00000674773.1:c.1681G>A	ENSP00000502579.1:p.Ala561Thr
ENST00000675517.1:c.1973G>A
ENST00000676076.1:c.1959G>A
ENST00000676260.1:c.2060G>A
ENST00000676316.1:c.1985G>A
XM_011527171.1:c.2098G>A	XP_011525473.1:p.Ala700Thr
XM_011527171.2:c.2098G>A	XP_011525473.1:p.Ala700Thr
XM_017027046.1:c.1996G>A	XP_016882535.1:p.Ala666Thr
XM_017027047.1:c.1996G>A	XP_016882536.1:p.Ala666Thr