Canonical Allele Identifier: CA802096

Gene: P3H1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42759319C>G , CM000663.2:g.42759319C>G	GRCh38
NC_000001.10:g.43224990C>G , CM000663.1:g.43224990C>G	GRCh37
NC_000001.9:g.42997577C>G	NCBI36
NG_008123.1:g.12766G>C , LRG_5:g.12766G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296388.10:c.690G>C MANE Select	ENSP00000296388.5:p.Ala230=
ENST00000236040.8:c.690G>C	ENSP00000236040.4:p.Ala230=
ENST00000296388.9:c.690G>C	ENSP00000296388.5:p.Ala230=
ENST00000372526.2:c.561G>C	ENSP00000361604.2:p.Ala187=
ENST00000397054.7:c.690G>C	ENSP00000380245.3:p.Ala230=
ENST00000460031.5:n.708G>C
ENST00000463465.1:n.156G>C
ENST00000495874.5:n.741G>C
NM_001146289.1:c.690G>C , LRG_5t2:c.690G>C	NP_001139761.1:p.Ala230=
NM_001243246.1:c.690G>C , LRG_5t3:c.690G>C	NP_001230175.1:p.Ala230=
NM_022356.3:c.690G>C , LRG_5t1:c.690G>C	NP_071751.3:p.Ala230=
XM_005271110.2:c.-319G>C	XP_005271167.1:n.-319G>C
XM_011541947.1:c.-341G>C	XP_011540249.1:n.-341G>C
XM_011541948.1:c.-341G>C	XP_011540250.1:n.-341G>C
XM_011541949.1:c.-341G>C	XP_011540251.1:n.-341G>C
XR_946739.1:n.747G>C
XM_017002051.2:c.-341G>C	XP_016857540.1:n.-341G>C
XM_017002052.2:c.-341G>C	XP_016857541.1:n.-341G>C
XR_946739.2:n.747G>C
NM_022356.4:c.690G>C MANE Select	NP_071751.3:p.Ala230=
NM_001146289.2:c.690G>C	NP_001139761.1:p.Ala230=
NM_001243246.2:c.690G>C	NP_001230175.1:p.Ala230=