Canonical Allele Identifier: CA2335960961

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395016T= , CM000681.2:g.40395016T=	GRCh38
NC_000019.9:g.40900923T= , CM000681.1:g.40900923T=	GRCh37
NC_000019.8:g.45592763T=	NCBI36
NG_007979.1:g.23349A= , LRG_265:g.23349A=
NG_051224.1:g.206A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3336A= MANE Select	ENSP00000326018.6:p.Ala1112=
ENST00000673881.1:c.2919A=	ENSP00000501070.1:p.Ala973=
ENST00000674005.2:c.3621A=	ENSP00000501261.1:p.Ala1207=
ENST00000674773.1:c.2919A=	ENSP00000502579.1:p.Ala973=
ENST00000675517.1:c.3211A=
ENST00000676076.1:c.3197A=
ENST00000676260.1:c.3298A=
ENST00000676316.1:c.3223A=
ENST00000291825.11:c.*3541A=	ENSP00000291825.6:n.*3541A=
ENST00000324001.7:c.3336A=	ENSP00000326018.6:p.Ala1112=
NM_020956.2:c.*3541A= , LRG_265t1:c.*3541A=	NP_066007.1:n.*3541A=
NM_181882.2:c.3336A= , LRG_265t2:c.3336A=	NP_870998.2:p.Ala1112=
XM_011527171.1:c.3336A=	XP_011525473.1:p.Ala1112=
XM_011527171.2:c.3336A=	XP_011525473.1:p.Ala1112=
XM_017027046.1:c.3234A=	XP_016882535.1:p.Ala1078=
XM_017027047.1:c.3234A=	XP_016882536.1:p.Ala1078=
NM_181882.3:c.3336A= MANE Select	NP_870998.2:p.Ala1112=