Canonical Allele Identifier: CA2335960947

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394993C= , CM000681.2:g.40394993C=	GRCh38
NC_000019.9:g.40900900C= , CM000681.1:g.40900900C=	GRCh37
NC_000019.8:g.45592740C=	NCBI36
NG_007979.1:g.23372G= , LRG_265:g.23372G=
NG_051224.1:g.229G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3359G= MANE Select	ENSP00000326018.6:p.Gly1120=
ENST00000673881.1:c.2942G=	ENSP00000501070.1:p.Gly981=
ENST00000674005.2:c.3644G=	ENSP00000501261.1:p.Gly1215=
ENST00000674773.1:c.2942G=	ENSP00000502579.1:p.Gly981=
ENST00000675517.1:c.3234G=
ENST00000676076.1:c.3220G=
ENST00000676260.1:c.3321G=
ENST00000676316.1:c.3246G=
ENST00000291825.11:c.*3564G=	ENSP00000291825.6:n.*3564G=
ENST00000324001.7:c.3359G=	ENSP00000326018.6:p.Gly1120=
NM_020956.2:c.*3564G= , LRG_265t1:c.*3564G=	NP_066007.1:n.*3564G=
NM_181882.2:c.3359G= , LRG_265t2:c.3359G=	NP_870998.2:p.Gly1120=
XM_011527171.1:c.3359G=	XP_011525473.1:p.Gly1120=
XM_011527171.2:c.3359G=	XP_011525473.1:p.Gly1120=
XM_017027046.1:c.3257G=	XP_016882535.1:p.Gly1086=
XM_017027047.1:c.3257G=	XP_016882536.1:p.Gly1086=
NM_181882.3:c.3359G= MANE Select	NP_870998.2:p.Gly1120=