Canonical Allele Identifier: CA801506

Gene: P3H1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42746754G>A , CM000663.2:g.42746754G>A	GRCh38
NC_000001.10:g.43212425G>A , CM000663.1:g.43212425G>A	GRCh37
NC_000001.9:g.42985012G>A	NCBI36
NG_008123.1:g.25331C>T , LRG_5:g.25331C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022356.4:c.2154C>T MANE Select	NP_071751.3:p.Pro718=
ENST00000296388.10:c.2154C>T MANE Select	ENSP00000296388.5:p.Pro718=
NM_001146289.1:c.*79C>T , LRG_5t2:c.*79C>T	NP_001139761.1:n.*79C>T
NM_001146289.2:c.*79C>T	NP_001139761.1:n.*79C>T
NM_001243246.1:c.*158C>T , LRG_5t3:c.*158C>T	NP_001230175.1:n.*158C>T
NM_001243246.2:c.*158C>T	NP_001230175.1:n.*158C>T
NM_022356.3:c.2154C>T , LRG_5t1:c.2154C>T	NP_071751.3:p.Pro718=
ENST00000236040.8:c.*158C>T	ENSP00000236040.4:n.*158C>T
ENST00000296388.9:c.2154C>T	ENSP00000296388.5:p.Pro718=
ENST00000397054.7:c.*79C>T	ENSP00000380245.3:n.*79C>T
ENST00000460031.5:n.2346C>T
ENST00000462474.5:n.335C>T
ENST00000472802.1:n.423C>T
ENST00000495874.5:n.2434C>T
XM_005271110.2:c.1146C>T	XP_005271167.1:p.Pro382=
XM_011541947.1:c.1179C>T	XP_011540249.1:p.Pro393=
XM_011541948.1:c.1179C>T	XP_011540250.1:p.Pro393=
XM_011541949.1:c.1176C>T	XP_011540251.1:p.Pro392=
XM_017002051.2:c.1179C>T	XP_016857540.1:p.Pro393=
XM_017002052.2:c.1176C>T	XP_016857541.1:p.Pro392=