Canonical Allele Identifier: CA1144360566
Gene: P3H1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42752645T= , CM000663.2:g.42752645T= GRCh38
NC_000001.10:g.43218316T= , CM000663.1:g.43218316T= GRCh37
NC_000001.9:g.42990903T= NCBI36
NG_008123.1:g.19440A= , LRG_5:g.19440A=

Transcript Alleles

HGVS Amino-acid change
ENST00000296388.10:c.1365A= MANE Select ENSP00000296388.5:p.Glu455=
ENST00000236040.8:c.1365A= ENSP00000236040.4:p.Glu455=
ENST00000296388.9:c.1365A= ENSP00000296388.5:p.Glu455=
ENST00000397054.7:c.1365A= ENSP00000380245.3:p.Glu455=
ENST00000431412.3:c.187A=
ENST00000447502.2:n.139A=
ENST00000460031.5:n.1557A=
ENST00000481465.3:n.88A=
ENST00000495874.5:n.1645A=
NM_001146289.1:c.1365A= , LRG_5t2:c.1365A= NP_001139761.1:p.Glu455=
NM_001243246.1:c.1365A= , LRG_5t3:c.1365A= NP_001230175.1:p.Glu455=
NM_022356.3:c.1365A= , LRG_5t1:c.1365A= NP_071751.3:p.Glu455=
XM_005271110.2:c.357A= XP_005271167.1:p.Glu119=
XM_011541947.1:c.390A= XP_011540249.1:p.Glu130=
XM_011541948.1:c.390A= XP_011540250.1:p.Glu130=
XM_011541949.1:c.387A= XP_011540251.1:p.Glu129=
XM_017002051.2:c.390A= XP_016857540.1:p.Glu130=
XM_017002052.2:c.387A= XP_016857541.1:p.Glu129=
XR_946739.2:n.1490A=
NM_022356.4:c.1365A= MANE Select NP_071751.3:p.Glu455=
NM_001146289.2:c.1365A= NP_001139761.1:p.Glu455=
NM_001243246.2:c.1365A= NP_001230175.1:p.Glu455=