Canonical Allele Identifier: CA2335961480

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396128G= , CM000681.2:g.40396128G=	GRCh38
NC_000019.9:g.40902035G= , CM000681.1:g.40902035G=	GRCh37
NC_000019.8:g.45593875G=	NCBI36
NG_007979.1:g.22237C= , LRG_265:g.22237C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2224C= MANE Select	ENSP00000326018.6:p.Leu742=
ENST00000673881.1:c.1807C=	ENSP00000501070.1:p.Leu603=
ENST00000674005.2:c.2509C=	ENSP00000501261.1:p.Leu837=
ENST00000674773.1:c.1807C=	ENSP00000502579.1:p.Leu603=
ENST00000675517.1:c.2099C=
ENST00000676076.1:c.2085C=
ENST00000676260.1:c.2186C=
ENST00000676316.1:c.2111C=
ENST00000291825.11:c.*2429C=	ENSP00000291825.6:n.*2429C=
ENST00000324001.7:c.2224C=	ENSP00000326018.6:p.Leu742=
NM_020956.2:c.*2429C= , LRG_265t1:c.*2429C=	NP_066007.1:n.*2429C=
NM_181882.2:c.2224C= , LRG_265t2:c.2224C=	NP_870998.2:p.Leu742=
XM_011527171.1:c.2224C=	XP_011525473.1:p.Leu742=
XM_011527171.2:c.2224C=	XP_011525473.1:p.Leu742=
XM_017027046.1:c.2122C=	XP_016882535.1:p.Leu708=
XM_017027047.1:c.2122C=	XP_016882536.1:p.Leu708=
NM_181882.3:c.2224C= MANE Select	NP_870998.2:p.Leu742=