Canonical Allele Identifier: CA801732

Gene: P3H1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42750190G>A , CM000663.2:g.42750190G>A	GRCh38
NC_000001.10:g.43215861G>A , CM000663.1:g.43215861G>A	GRCh37
NC_000001.9:g.42988448G>A	NCBI36
NG_008123.1:g.21895C>T , LRG_5:g.21895C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296388.10:c.1716C>T MANE Select	ENSP00000296388.5:p.Ile572=
ENST00000236040.8:c.1716C>T	ENSP00000236040.4:p.Ile572=
ENST00000296388.9:c.1716C>T	ENSP00000296388.5:p.Ile572=
ENST00000397054.7:c.1716C>T	ENSP00000380245.3:p.Ile572=
ENST00000431412.3:c.638C>T
ENST00000460031.5:n.1908C>T
ENST00000481465.3:n.439C>T
ENST00000495874.5:n.1996C>T
NM_001146289.1:c.1716C>T , LRG_5t2:c.1716C>T	NP_001139761.1:p.Ile572=
NM_001243246.1:c.1716C>T , LRG_5t3:c.1716C>T	NP_001230175.1:p.Ile572=
NM_022356.3:c.1716C>T , LRG_5t1:c.1716C>T	NP_071751.3:p.Ile572=
XM_005271110.2:c.708C>T	XP_005271167.1:p.Ile236=
XM_011541947.1:c.741C>T	XP_011540249.1:p.Ile247=
XM_011541948.1:c.741C>T	XP_011540250.1:p.Ile247=
XM_011541949.1:c.738C>T	XP_011540251.1:p.Ile246=
XM_017002051.2:c.741C>T	XP_016857540.1:p.Ile247=
XM_017002052.2:c.738C>T	XP_016857541.1:p.Ile246=
XR_946739.2:n.1841C>T
NM_022356.4:c.1716C>T MANE Select	NP_071751.3:p.Ile572=
NM_001146289.2:c.1716C>T	NP_001139761.1:p.Ile572=
NM_001243246.2:c.1716C>T	NP_001230175.1:p.Ile572=