Canonical Allele Identifier: CA2335960919

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394933T= , CM000681.2:g.40394933T=	GRCh38
NC_000019.9:g.40900840T= , CM000681.1:g.40900840T=	GRCh37
NC_000019.8:g.45592680T=	NCBI36
NG_007979.1:g.23432A= , LRG_265:g.23432A=
NG_051224.1:g.289A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3419A= MANE Select	ENSP00000326018.6:p.Asp1140=
ENST00000673881.1:c.3002A=	ENSP00000501070.1:p.Asp1001=
ENST00000674005.2:c.3704A=	ENSP00000501261.1:p.Asp1235=
ENST00000674773.1:c.3002A=	ENSP00000502579.1:p.Asp1001=
ENST00000675517.1:c.3294A=
ENST00000676076.1:c.3280A=
ENST00000676260.1:c.3381A=
ENST00000676316.1:c.3306A=
ENST00000291825.11:c.*3624A=	ENSP00000291825.6:n.*3624A=
ENST00000324001.7:c.3419A=	ENSP00000326018.6:p.Asp1140=
NM_020956.2:c.*3624A= , LRG_265t1:c.*3624A=	NP_066007.1:n.*3624A=
NM_181882.2:c.3419A= , LRG_265t2:c.3419A=	NP_870998.2:p.Asp1140=
XM_011527171.1:c.3419A=	XP_011525473.1:p.Asp1140=
XM_011527171.2:c.3419A=	XP_011525473.1:p.Asp1140=
XM_017027046.1:c.3317A=	XP_016882535.1:p.Asp1106=
XM_017027047.1:c.3317A=	XP_016882536.1:p.Asp1106=
NM_181882.3:c.3419A= MANE Select	NP_870998.2:p.Asp1140=