Canonical Allele Identifier: CA801693

Gene: P3H1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42748226G>A , CM000663.2:g.42748226G>A	GRCh38
NC_000001.10:g.43213897G>A , CM000663.1:g.43213897G>A	GRCh37
NC_000001.9:g.42986484G>A	NCBI36
NG_008123.1:g.23859C>T , LRG_5:g.23859C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296388.10:c.1812C>T MANE Select	ENSP00000296388.5:p.Pro604=
ENST00000236040.8:c.1812C>T	ENSP00000236040.4:p.Pro604=
ENST00000296388.9:c.1812C>T	ENSP00000296388.5:p.Pro604=
ENST00000397054.7:c.1812C>T	ENSP00000380245.3:p.Pro604=
ENST00000431412.3:c.734C>T
ENST00000460031.5:n.2004C>T
ENST00000460831.1:n.518C>T
ENST00000495874.5:n.2092C>T
NM_001146289.1:c.1812C>T , LRG_5t2:c.1812C>T	NP_001139761.1:p.Pro604=
NM_001243246.1:c.1812C>T , LRG_5t3:c.1812C>T	NP_001230175.1:p.Pro604=
NM_022356.3:c.1812C>T , LRG_5t1:c.1812C>T	NP_071751.3:p.Pro604=
XM_005271110.2:c.804C>T	XP_005271167.1:p.Pro268=
XM_011541947.1:c.837C>T	XP_011540249.1:p.Pro279=
XM_011541948.1:c.837C>T	XP_011540250.1:p.Pro279=
XM_011541949.1:c.834C>T	XP_011540251.1:p.Pro278=
XM_017002051.2:c.837C>T	XP_016857540.1:p.Pro279=
XM_017002052.2:c.834C>T	XP_016857541.1:p.Pro278=
XR_946739.2:n.1937C>T
NM_022356.4:c.1812C>T MANE Select	NP_071751.3:p.Pro604=
NM_001146289.2:c.1812C>T	NP_001139761.1:p.Pro604=
NM_001243246.2:c.1812C>T	NP_001230175.1:p.Pro604=