Canonical Allele Identifier: CA1891553351

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13298209T= , CM000672.2:g.13298209T=	GRCh38
NC_000010.10:g.13340209T= , CM000672.1:g.13340209T=	GRCh37
NC_000010.9:g.13380215T=	NCBI36
NG_012862.1:g.6922A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.112A= MANE Select	ENSP00000263038.4:p.Ser38=
ENST00000263038.8:c.112A=	ENSP00000263038.4:p.Ser38=
ENST00000396913.6:c.-167+1211A=	ENSP00000380121.2:n.-167+1211A=
ENST00000396920.7:c.55A=	ENSP00000380126.3:p.Ser19=
ENST00000453759.6:c.-189A=	ENSP00000412525.2:n.-189A=
ENST00000463730.1:n.167A=
ENST00000479604.1:c.112A=	ENSP00000420117.1:p.Ser38=
NM_001037537.1:c.-167+1211A=	NP_001032626.1:n.-167+1211A=
NM_006214.3:c.112A=	NP_006205.1:p.Ser38=
XM_005252469.2:c.157A=	XP_005252526.1:p.Ser53=
NM_001323080.1:c.-189A=	NP_001310009.1:n.-189A=
NM_001323082.1:c.112A=	NP_001310011.1:p.Ser38=
NM_001323083.1:c.112A=	NP_001310012.1:p.Ser38=
NM_001323084.1:c.-167+1211A=	NP_001310013.1:n.-167+1211A=
NM_006214.4:c.112A= MANE Select	NP_006205.1:p.Ser38=
NM_001037537.2:c.-167+1211A=	NP_001032626.1:n.-167+1211A=
NM_001323080.2:c.-189A=	NP_001310009.1:n.-189A=
NM_001323082.2:c.112A=	NP_001310011.1:p.Ser38=
NM_001323083.2:c.112A=	NP_001310012.1:p.Ser38=
NM_001323084.2:c.-167+1211A=	NP_001310013.1:n.-167+1211A=