Canonical Allele Identifier: CA2335960911

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394921C= , CM000681.2:g.40394921C=	GRCh38
NC_000019.9:g.40900828C= , CM000681.1:g.40900828C=	GRCh37
NC_000019.8:g.45592668C=	NCBI36
NG_007979.1:g.23444G= , LRG_265:g.23444G=
NG_051224.1:g.301G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.3431G= MANE Select	ENSP00000326018.6:p.Arg1144=
ENST00000673881.1:c.3014G=	ENSP00000501070.1:p.Arg1005=
ENST00000674005.2:c.3716G=	ENSP00000501261.1:p.Arg1239=
ENST00000674773.1:c.3014G=	ENSP00000502579.1:p.Arg1005=
ENST00000675517.1:c.3306G=
ENST00000676076.1:c.3292G=
ENST00000676260.1:c.3393G=
ENST00000676316.1:c.3318G=
ENST00000291825.11:c.*3636G=	ENSP00000291825.6:n.*3636G=
ENST00000324001.7:c.3431G=	ENSP00000326018.6:p.Arg1144=
NM_020956.2:c.*3636G= , LRG_265t1:c.*3636G=	NP_066007.1:n.*3636G=
NM_181882.2:c.3431G= , LRG_265t2:c.3431G=	NP_870998.2:p.Arg1144=
XM_011527171.1:c.3431G=	XP_011525473.1:p.Arg1144=
XM_011527171.2:c.3431G=	XP_011525473.1:p.Arg1144=
XM_017027046.1:c.3329G=	XP_016882535.1:p.Arg1110=
XM_017027047.1:c.3329G=	XP_016882536.1:p.Arg1110=
NM_181882.3:c.3431G= MANE Select	NP_870998.2:p.Arg1144=