Canonical Allele Identifier: CA1428574770

Gene: P3H2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995378A= , CM000665.2:g.189995378A=	GRCh38
NC_000003.11:g.189713167A= , CM000665.1:g.189713167A=	GRCh37
NC_000003.10:g.191195861A=	NCBI36
NG_031929.1:g.132060T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000319332.10:c.545T= MANE Select	ENSP00000316881.5:p.Met182=
ENST00000319332.9:c.545T=	ENSP00000316881.5:p.Met182=
ENST00000426003.1:c.2T=	ENSP00000394326.1:p.Met1=
ENST00000427335.6:c.2T=	ENSP00000408947.2:p.Met1=
ENST00000444866.5:c.2T=	ENSP00000391374.1:p.Met1=
NM_001134418.1:c.2T=	NP_001127890.1:p.Met1=
NM_018192.3:c.545T=	NP_060662.2:p.Met182=
XM_011512955.1:c.2T=	XP_011511257.1:p.Met1=
NM_018192.4:c.545T= MANE Select	NP_060662.2:p.Met182=
NM_001134418.2:c.2T=	NP_001127890.1:p.Met1=