Canonical Allele Identifier: CA1891546513

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283765C= , CM000672.2:g.13283765C=	GRCh38
NC_000010.10:g.13325765C= , CM000672.1:g.13325765C=	GRCh37
NC_000010.9:g.13365771C=	NCBI36
NG_012862.1:g.21366G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.753G= MANE Select	ENSP00000263038.4:p.Glu251=
ENST00000263038.8:c.753G=	ENSP00000263038.4:p.Glu251=
ENST00000396913.6:c.453G=	ENSP00000380121.2:p.Glu151=
ENST00000396920.7:c.702G=	ENSP00000380126.3:p.Glu234=
ENST00000453759.6:c.453G=	ENSP00000412525.2:p.Glu151=
NM_001037537.1:c.453G=	NP_001032626.1:p.Glu151=
NM_006214.3:c.753G=	NP_006205.1:p.Glu251=
XM_005252469.2:c.534G=	XP_005252526.1:p.Glu178=
NM_001323080.1:c.453G=	NP_001310009.1:p.Glu151=
NM_001323082.1:c.759G=	NP_001310011.1:p.Glu253=
NM_001323083.1:c.489G=	NP_001310012.1:p.Glu163=
NM_001323084.1:c.459G=	NP_001310013.1:p.Glu153=
NM_006214.4:c.753G= MANE Select	NP_006205.1:p.Glu251=
NM_001037537.2:c.453G=	NP_001032626.1:p.Glu151=
NM_001323080.2:c.453G=	NP_001310009.1:p.Glu151=
NM_001323082.2:c.759G=	NP_001310011.1:p.Glu253=
NM_001323083.2:c.489G=	NP_001310012.1:p.Glu163=
NM_001323084.2:c.459G=	NP_001310013.1:p.Glu153=