Canonical Allele Identifier: CA1428574696

Gene: P3H2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995355T= , CM000665.2:g.189995355T=	GRCh38
NC_000003.11:g.189713144T= , CM000665.1:g.189713144T=	GRCh37
NC_000003.10:g.191195838T=	NCBI36
NG_031929.1:g.132083A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.568A= MANE Select	ENSP00000316881.5:p.Asn190=
ENST00000319332.9:c.568A=	ENSP00000316881.5:p.Asn190=
ENST00000426003.1:c.25A=	ENSP00000394326.1:p.Asn9=
ENST00000427335.6:c.25A=	ENSP00000408947.2:p.Asn9=
ENST00000444866.5:c.25A=	ENSP00000391374.1:p.Asn9=
NM_001134418.1:c.25A=	NP_001127890.1:p.Asn9=
NM_018192.3:c.568A=	NP_060662.2:p.Asn190=
XM_011512955.1:c.25A=	XP_011511257.1:p.Asn9=
NM_018192.4:c.568A= MANE Select	NP_060662.2:p.Asn190=
NM_001134418.2:c.25A=	NP_001127890.1:p.Asn9=