Canonical Allele Identifier: CA2335961411

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396007A= , CM000681.2:g.40396007A=	GRCh38
NC_000019.9:g.40901914A= , CM000681.1:g.40901914A=	GRCh37
NC_000019.8:g.45593754A=	NCBI36
NG_007979.1:g.22358T= , LRG_265:g.22358T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2345T= MANE Select	ENSP00000326018.6:p.Val782=
ENST00000673881.1:c.1928T=	ENSP00000501070.1:p.Val643=
ENST00000674005.2:c.2630T=	ENSP00000501261.1:p.Val877=
ENST00000674773.1:c.1928T=	ENSP00000502579.1:p.Val643=
ENST00000675517.1:c.2220T=
ENST00000676076.1:c.2206T=
ENST00000676260.1:c.2307T=
ENST00000676316.1:c.2232T=
ENST00000291825.11:c.*2550T=	ENSP00000291825.6:n.*2550T=
ENST00000324001.7:c.2345T=	ENSP00000326018.6:p.Val782=
NM_020956.2:c.*2550T= , LRG_265t1:c.*2550T=	NP_066007.1:n.*2550T=
NM_181882.2:c.2345T= , LRG_265t2:c.2345T=	NP_870998.2:p.Val782=
XM_011527171.1:c.2345T=	XP_011525473.1:p.Val782=
XM_011527171.2:c.2345T=	XP_011525473.1:p.Val782=
XM_017027046.1:c.2243T=	XP_016882535.1:p.Val748=
XM_017027047.1:c.2243T=	XP_016882536.1:p.Val748=
NM_181882.3:c.2345T= MANE Select	NP_870998.2:p.Val782=