Canonical Allele Identifier: CA802028

Gene: P3H1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42758851C>A , CM000663.2:g.42758851C>A	GRCh38
NC_000001.10:g.43224522C>A , CM000663.1:g.43224522C>A	GRCh37
NC_000001.9:g.42997109C>A	NCBI36
NG_008123.1:g.13234G>T , LRG_5:g.13234G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022356.4:c.940+1G>T MANE Select	NP_071751.3:n.940+1G>T
ENST00000296388.10:c.940+1G>T MANE Select	ENSP00000296388.5:n.940+1G>T
NM_001146289.1:c.940+1G>T , LRG_5t2:c.940+1G>T	NP_001139761.1:n.940+1G>T
NM_001146289.2:c.940+1G>T	NP_001139761.1:n.940+1G>T
NM_001243246.1:c.940+1G>T , LRG_5t3:c.940+1G>T	NP_001230175.1:n.940+1G>T
NM_001243246.2:c.940+1G>T	NP_001230175.1:n.940+1G>T
NM_022356.3:c.940+1G>T , LRG_5t1:c.940+1G>T	NP_071751.3:n.940+1G>T
ENST00000236040.8:c.940+1G>T	ENSP00000236040.4:n.940+1G>T
ENST00000296388.9:c.940+1G>T	ENSP00000296388.5:n.940+1G>T
ENST00000397054.7:c.940+1G>T	ENSP00000380245.3:n.940+1G>T
ENST00000460031.5:n.958+1G>T
ENST00000463465.1:n.406+1G>T
ENST00000495874.5:n.991+1G>T
XM_005271110.2:c.-69+1G>T	XP_005271167.1:n.-69+1G>T
XM_011541947.1:c.-91+1G>T	XP_011540249.1:n.-91+1G>T
XM_011541948.1:c.-91+1G>T	XP_011540250.1:n.-91+1G>T
XM_011541949.1:c.-91+1G>T	XP_011540251.1:n.-91+1G>T
XM_017002051.2:c.-91+1G>T	XP_016857540.1:n.-91+1G>T
XM_017002052.2:c.-91+1G>T	XP_016857541.1:n.-91+1G>T
XR_946739.1:n.997+1G>T
XR_946739.2:n.997+1G>T