Canonical Allele Identifier: CA2335960916

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394930G= , CM000681.2:g.40394930G=	GRCh38
NC_000019.9:g.40900837G= , CM000681.1:g.40900837G=	GRCh37
NC_000019.8:g.45592677G=	NCBI36
NG_007979.1:g.23435C= , LRG_265:g.23435C=
NG_051224.1:g.292C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3422C= MANE Select	ENSP00000326018.6:p.Ala1141=
ENST00000673881.1:c.3005C=	ENSP00000501070.1:p.Ala1002=
ENST00000674005.2:c.3707C=	ENSP00000501261.1:p.Ala1236=
ENST00000674773.1:c.3005C=	ENSP00000502579.1:p.Ala1002=
ENST00000675517.1:c.3297C=
ENST00000676076.1:c.3283C=
ENST00000676260.1:c.3384C=
ENST00000676316.1:c.3309C=
ENST00000291825.11:c.*3627C=	ENSP00000291825.6:n.*3627C=
ENST00000324001.7:c.3422C=	ENSP00000326018.6:p.Ala1141=
NM_020956.2:c.*3627C= , LRG_265t1:c.*3627C=	NP_066007.1:n.*3627C=
NM_181882.2:c.3422C= , LRG_265t2:c.3422C=	NP_870998.2:p.Ala1141=
XM_011527171.1:c.3422C=	XP_011525473.1:p.Ala1141=
XM_011527171.2:c.3422C=	XP_011525473.1:p.Ala1141=
XM_017027046.1:c.3320C=	XP_016882535.1:p.Ala1107=
XM_017027047.1:c.3320C=	XP_016882536.1:p.Ala1107=
NM_181882.3:c.3422C= MANE Select	NP_870998.2:p.Ala1141=