Canonical Allele Identifier: CA3181751539

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283731T= , CM000672.2:g.13283731T=	GRCh38
NC_000010.10:g.13325731T= , CM000672.1:g.13325731T=	GRCh37
NC_000010.9:g.13365737T=	NCBI36
NG_012862.1:g.21400A=

Transcript Alleles

HGVS	Amino-acid Change
NM_006214.4:c.787A= MANE Select	NP_006205.1:p.Ile263=
ENST00000263038.9:c.787A= MANE Select	ENSP00000263038.4:p.Ile263=
NM_001037537.1:c.487A=	NP_001032626.1:p.Ile163=
NM_001037537.2:c.487A=	NP_001032626.1:p.Ile163=
NM_001323080.1:c.487A=	NP_001310009.1:p.Ile163=
NM_001323080.2:c.487A=	NP_001310009.1:p.Ile163=
NM_001323082.1:c.793A=	NP_001310011.1:p.Ile265=
NM_001323082.2:c.793A=	NP_001310011.1:p.Ile265=
NM_001323083.1:c.523A=	NP_001310012.1:p.Ile175=
NM_001323083.2:c.523A=	NP_001310012.1:p.Ile175=
NM_001323084.1:c.493A=	NP_001310013.1:p.Ile165=
NM_001323084.2:c.493A=	NP_001310013.1:p.Ile165=
NM_006214.3:c.787A=	NP_006205.1:p.Ile263=
ENST00000263038.8:c.787A=	ENSP00000263038.4:p.Ile263=
ENST00000396913.6:c.487A=	ENSP00000380121.2:p.Ile163=
ENST00000396920.7:c.736A=	ENSP00000380126.3:p.Ile246=
ENST00000453759.6:c.487A=	ENSP00000412525.2:p.Ile163=
XM_005252469.2:c.568A=	XP_005252526.1:p.Ile190=