Canonical Allele Identifier: CA2335960859

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394824T= , CM000681.2:g.40394824T=	GRCh38
NC_000019.9:g.40900731T= , CM000681.1:g.40900731T=	GRCh37
NC_000019.8:g.45592571T=	NCBI36
NG_007979.1:g.23541A= , LRG_265:g.23541A=
NG_051224.1:g.398A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3528A= MANE Select	ENSP00000326018.6:p.Ser1176=
ENST00000673881.1:c.3111A=	ENSP00000501070.1:p.Ser1037=
ENST00000674005.2:c.3813A=	ENSP00000501261.1:p.Ser1271=
ENST00000674773.1:c.3111A=	ENSP00000502579.1:p.Ser1037=
ENST00000675517.1:c.3403A=
ENST00000676076.1:c.3389A=
ENST00000676260.1:c.3490A=
ENST00000676316.1:c.3415A=
ENST00000291825.11:c.*3733A=	ENSP00000291825.6:n.*3733A=
ENST00000324001.7:c.3528A=	ENSP00000326018.6:p.Ser1176=
NM_020956.2:c.*3733A= , LRG_265t1:c.*3733A=	NP_066007.1:n.*3733A=
NM_181882.2:c.3528A= , LRG_265t2:c.3528A=	NP_870998.2:p.Ser1176=
XM_011527171.1:c.3528A=	XP_011525473.1:p.Ser1176=
XM_011527171.2:c.3528A=	XP_011525473.1:p.Ser1176=
XM_017027046.1:c.3426A=	XP_016882535.1:p.Ser1142=
XM_017027047.1:c.3426A=	XP_016882536.1:p.Ser1142=
NM_181882.3:c.3528A= MANE Select	NP_870998.2:p.Ser1176=