Canonical Allele Identifier: CA1891546668

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283826T= , CM000672.2:g.13283826T=	GRCh38
NC_000010.10:g.13325826T= , CM000672.1:g.13325826T=	GRCh37
NC_000010.9:g.13365832T=	NCBI36
NG_012862.1:g.21305A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.692A= MANE Select	ENSP00000263038.4:p.Lys231=
ENST00000263038.8:c.692A=	ENSP00000263038.4:p.Lys231=
ENST00000396913.6:c.392A=	ENSP00000380121.2:p.Lys131=
ENST00000396920.7:c.641A=	ENSP00000380126.3:p.Lys214=
ENST00000453759.6:c.392A=	ENSP00000412525.2:p.Lys131=
NM_001037537.1:c.392A=	NP_001032626.1:p.Lys131=
NM_006214.3:c.692A=	NP_006205.1:p.Lys231=
XM_005252469.2:c.473A=	XP_005252526.1:p.Lys158=
NM_001323080.1:c.392A=	NP_001310009.1:p.Lys131=
NM_001323082.1:c.698A=	NP_001310011.1:p.Lys233=
NM_001323083.1:c.428A=	NP_001310012.1:p.Lys143=
NM_001323084.1:c.398A=	NP_001310013.1:p.Lys133=
NM_006214.4:c.692A= MANE Select	NP_006205.1:p.Lys231=
NM_001037537.2:c.392A=	NP_001032626.1:p.Lys131=
NM_001323080.2:c.392A=	NP_001310009.1:p.Lys131=
NM_001323082.2:c.698A=	NP_001310011.1:p.Lys233=
NM_001323083.2:c.428A=	NP_001310012.1:p.Lys143=
NM_001323084.2:c.398A=	NP_001310013.1:p.Lys133=