Canonical Allele Identifier: CA2335960327

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40393775A= , CM000681.2:g.40393775A=	GRCh38
NC_000019.9:g.40899682A= , CM000681.1:g.40899682A=	GRCh37
NC_000019.8:g.45591522A=	NCBI36
NG_007979.1:g.24590T= , LRG_265:g.24590T=
NG_051224.1:g.1447T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.*191T= MANE Select	ENSP00000326018.6:n.*191T=
ENST00000673881.1:c.*191T=	ENSP00000501070.1:n.*191T=
ENST00000674005.2:c.*191T=	ENSP00000501261.1:n.*191T=
ENST00000674773.1:c.*191T=	ENSP00000502579.1:n.*191T=
ENST00000676076.1:c.4438T=
ENST00000676316.1:c.4464T=
ENST00000291825.11:c.*4782T=	ENSP00000291825.6:n.*4782T=
ENST00000324001.7:c.*191T=	ENSP00000326018.6:n.*191T=
NM_020956.2:c.*4782T= , LRG_265t1:c.*4782T=	NP_066007.1:n.*4782T=
NM_181882.2:c.*191T= , LRG_265t2:c.*191T=	NP_870998.2:n.*191T=
XM_011527171.1:c.*191T=	XP_011525473.1:n.*191T=
XM_011527171.2:c.*191T=	XP_011525473.1:n.*191T=
XM_017027046.1:c.*191T=	XP_016882535.1:n.*191T=
XM_017027047.1:c.*191T=	XP_016882536.1:n.*191T=
NM_181882.3:c.*191T= MANE Select	NP_870998.2:n.*191T=