Canonical Allele Identifier: CA339963411

Gene: P3H1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42766524G>A , CM000663.2:g.42766524G>A	GRCh38
NC_000001.10:g.43232195G>A , CM000663.1:g.43232195G>A	GRCh37
NC_000001.9:g.43004782G>A	NCBI36
NG_008123.1:g.5561C>T , LRG_5:g.5561C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022356.4:c.448C>T MANE Select	NP_071751.3:p.Gln150Ter
ENST00000296388.10:c.448C>T MANE Select	ENSP00000296388.5:p.Gln150Ter
NM_001146289.1:c.448C>T , LRG_5t2:c.448C>T	NP_001139761.1:p.Gln150Ter
NM_001146289.2:c.448C>T	NP_001139761.1:p.Gln150Ter
NM_001243246.1:c.448C>T , LRG_5t3:c.448C>T	NP_001230175.1:p.Gln150Ter
NM_001243246.2:c.448C>T	NP_001230175.1:p.Gln150Ter
NM_022356.3:c.448C>T , LRG_5t1:c.448C>T	NP_071751.3:p.Gln150Ter
ENST00000236040.8:c.448C>T	ENSP00000236040.4:p.Gln150Ter
ENST00000296388.9:c.448C>T	ENSP00000296388.5:p.Gln150Ter
ENST00000372526.2:c.448C>T	ENSP00000361604.2:p.Gln150Ter
ENST00000397054.7:c.448C>T	ENSP00000380245.3:p.Gln150Ter
ENST00000460031.5:n.466C>T
ENST00000492956.1:n.494C>T
ENST00000495874.5:n.499C>T
XM_017002051.2:c.-583C>T	XP_016857540.1:n.-583C>T
XM_017002052.2:c.-583C>T	XP_016857541.1:n.-583C>T
XR_946739.1:n.505C>T
XR_946739.2:n.505C>T