Canonical Allele Identifier: CA801951

Gene: P3H1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42755543C>G , CM000663.2:g.42755543C>G	GRCh38
NC_000001.10:g.43221214C>G , CM000663.1:g.43221214C>G	GRCh37
NC_000001.9:g.42993801C>G	NCBI36
NG_008123.1:g.16542G>C , LRG_5:g.16542G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_022356.4:c.1170+5G>C MANE Select	NP_071751.3:n.1170+5G>C
ENST00000296388.10:c.1170+5G>C MANE Select	ENSP00000296388.5:n.1170+5G>C
NM_001146289.1:c.1170+5G>C , LRG_5t2:c.1170+5G>C	NP_001139761.1:n.1170+5G>C
NM_001146289.2:c.1170+5G>C	NP_001139761.1:n.1170+5G>C
NM_001243246.1:c.1170+5G>C , LRG_5t3:c.1170+5G>C	NP_001230175.1:n.1170+5G>C
NM_001243246.2:c.1170+5G>C	NP_001230175.1:n.1170+5G>C
NM_022356.3:c.1170+5G>C , LRG_5t1:c.1170+5G>C	NP_071751.3:n.1170+5G>C
ENST00000236040.8:c.1170+5G>C	ENSP00000236040.4:n.1170+5G>C
ENST00000296388.9:c.1170+5G>C	ENSP00000296388.5:n.1170+5G>C
ENST00000397054.7:c.1170+5G>C	ENSP00000380245.3:n.1170+5G>C
ENST00000460031.5:n.1188+5G>C
ENST00000463465.1:n.659+5G>C
ENST00000495874.5:n.1276+5G>C
XM_005271110.2:c.162+5G>C	XP_005271167.1:n.162+5G>C
XM_011541947.1:c.195+5G>C	XP_011540249.1:n.195+5G>C
XM_011541948.1:c.195+5G>C	XP_011540250.1:n.195+5G>C
XM_011541949.1:c.192+5G>C	XP_011540251.1:n.192+5G>C
XM_017002051.2:c.195+5G>C	XP_016857540.1:n.195+5G>C
XM_017002052.2:c.192+5G>C	XP_016857541.1:n.192+5G>C
XR_946739.1:n.1227+5G>C
XR_946739.2:n.1227+5G>C