Canonical Allele Identifier: CA1428574532

Gene: P3H2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995272G= , CM000665.2:g.189995272G=	GRCh38
NC_000003.11:g.189713061G= , CM000665.1:g.189713061G=	GRCh37
NC_000003.10:g.191195755G=	NCBI36
NG_031929.1:g.132166C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.633+18C= MANE Select	ENSP00000316881.5:n.633+18C=
ENST00000319332.9:c.633+18C=	ENSP00000316881.5:n.633+18C=
ENST00000426003.1:c.90+18C=	ENSP00000394326.1:n.90+18C=
ENST00000427335.6:c.90+18C=	ENSP00000408947.2:n.90+18C=
ENST00000444866.5:c.90+18C=	ENSP00000391374.1:n.90+18C=
NM_001134418.1:c.90+18C=	NP_001127890.1:n.90+18C=
NM_018192.3:c.633+18C=	NP_060662.2:n.633+18C=
XM_011512955.1:c.90+18C=	XP_011511257.1:n.90+18C=
NM_018192.4:c.633+18C= MANE Select	NP_060662.2:n.633+18C=
NM_001134418.2:c.90+18C=	NP_001127890.1:n.90+18C=