Canonical Allele Identifier: CA2335961559

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396281T= , CM000681.2:g.40396281T=	GRCh38
NC_000019.9:g.40902188T= , CM000681.1:g.40902188T=	GRCh37
NC_000019.8:g.45594028T=	NCBI36
NG_007979.1:g.22084A= , LRG_265:g.22084A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2071A= MANE Select	ENSP00000326018.6:p.Met691=
ENST00000673881.1:c.1654A=	ENSP00000501070.1:p.Met552=
ENST00000674005.2:c.2356A=	ENSP00000501261.1:p.Met786=
ENST00000674773.1:c.1654A=	ENSP00000502579.1:p.Met552=
ENST00000675517.1:c.1946A=
ENST00000676076.1:c.1932A=
ENST00000676260.1:c.2033A=
ENST00000676316.1:c.1958A=
ENST00000291825.11:c.*2276A=	ENSP00000291825.6:n.*2276A=
ENST00000324001.7:c.2071A=	ENSP00000326018.6:p.Met691=
NM_020956.2:c.*2276A= , LRG_265t1:c.*2276A=	NP_066007.1:n.*2276A=
NM_181882.2:c.2071A= , LRG_265t2:c.2071A=	NP_870998.2:p.Met691=
XM_011527171.1:c.2071A=	XP_011525473.1:p.Met691=
XM_011527171.2:c.2071A=	XP_011525473.1:p.Met691=
XM_017027046.1:c.1969A=	XP_016882535.1:p.Met657=
XM_017027047.1:c.1969A=	XP_016882536.1:p.Met657=
NM_181882.3:c.2071A= MANE Select	NP_870998.2:p.Met691=