Canonical Allele Identifier: CA2335961410

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395999T= , CM000681.2:g.40395999T=	GRCh38
NC_000019.9:g.40901906T= , CM000681.1:g.40901906T=	GRCh37
NC_000019.8:g.45593746T=	NCBI36
NG_007979.1:g.22366A= , LRG_265:g.22366A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2353A= MANE Select	ENSP00000326018.6:p.Lys785=
ENST00000673881.1:c.1936A=	ENSP00000501070.1:p.Lys646=
ENST00000674005.2:c.2638A=	ENSP00000501261.1:p.Lys880=
ENST00000674773.1:c.1936A=	ENSP00000502579.1:p.Lys646=
ENST00000675517.1:c.2228A=
ENST00000676076.1:c.2214A=
ENST00000676260.1:c.2315A=
ENST00000676316.1:c.2240A=
ENST00000291825.11:c.*2558A=	ENSP00000291825.6:n.*2558A=
ENST00000324001.7:c.2353A=	ENSP00000326018.6:p.Lys785=
NM_020956.2:c.*2558A= , LRG_265t1:c.*2558A=	NP_066007.1:n.*2558A=
NM_181882.2:c.2353A= , LRG_265t2:c.2353A=	NP_870998.2:p.Lys785=
XM_011527171.1:c.2353A=	XP_011525473.1:p.Lys785=
XM_011527171.2:c.2353A=	XP_011525473.1:p.Lys785=
XM_017027046.1:c.2251A=	XP_016882535.1:p.Lys751=
XM_017027047.1:c.2251A=	XP_016882536.1:p.Lys751=
NM_181882.3:c.2353A= MANE Select	NP_870998.2:p.Lys785=