Canonical Allele Identifier: CA1891546511

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283763T= , CM000672.2:g.13283763T=	GRCh38
NC_000010.10:g.13325763T= , CM000672.1:g.13325763T=	GRCh37
NC_000010.9:g.13365769T=	NCBI36
NG_012862.1:g.21368A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.755A= MANE Select	ENSP00000263038.4:p.Lys252=
ENST00000263038.8:c.755A=	ENSP00000263038.4:p.Lys252=
ENST00000396913.6:c.455A=	ENSP00000380121.2:p.Lys152=
ENST00000396920.7:c.704A=	ENSP00000380126.3:p.Lys235=
ENST00000453759.6:c.455A=	ENSP00000412525.2:p.Lys152=
NM_001037537.1:c.455A=	NP_001032626.1:p.Lys152=
NM_006214.3:c.755A=	NP_006205.1:p.Lys252=
XM_005252469.2:c.536A=	XP_005252526.1:p.Lys179=
NM_001323080.1:c.455A=	NP_001310009.1:p.Lys152=
NM_001323082.1:c.761A=	NP_001310011.1:p.Lys254=
NM_001323083.1:c.491A=	NP_001310012.1:p.Lys164=
NM_001323084.1:c.461A=	NP_001310013.1:p.Lys154=
NM_006214.4:c.755A= MANE Select	NP_006205.1:p.Lys252=
NM_001037537.2:c.455A=	NP_001032626.1:p.Lys152=
NM_001323080.2:c.455A=	NP_001310009.1:p.Lys152=
NM_001323082.2:c.761A=	NP_001310011.1:p.Lys254=
NM_001323083.2:c.491A=	NP_001310012.1:p.Lys164=
NM_001323084.2:c.461A=	NP_001310013.1:p.Lys154=