Canonical Allele Identifier: CA1891546393

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283692T= , CM000672.2:g.13283692T=	GRCh38
NC_000010.10:g.13325692T= , CM000672.1:g.13325692T=	GRCh37
NC_000010.9:g.13365698T=	NCBI36
NG_012862.1:g.21439A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.826A= MANE Select	ENSP00000263038.4:p.Lys276=
ENST00000263038.8:c.826A=	ENSP00000263038.4:p.Lys276=
ENST00000396913.6:c.526A=	ENSP00000380121.2:p.Lys176=
ENST00000396920.7:c.775A=	ENSP00000380126.3:p.Lys259=
ENST00000453759.6:c.526A=	ENSP00000412525.2:p.Lys176=
NM_001037537.1:c.526A=	NP_001032626.1:p.Lys176=
NM_006214.3:c.826A=	NP_006205.1:p.Lys276=
XM_005252469.2:c.607A=	XP_005252526.1:p.Lys203=
NM_001323080.1:c.526A=	NP_001310009.1:p.Lys176=
NM_001323082.1:c.832A=	NP_001310011.1:p.Lys278=
NM_001323083.1:c.562A=	NP_001310012.1:p.Lys188=
NM_001323084.1:c.532A=	NP_001310013.1:p.Lys178=
NM_006214.4:c.826A= MANE Select	NP_006205.1:p.Lys276=
NM_001037537.2:c.526A=	NP_001032626.1:p.Lys176=
NM_001323080.2:c.526A=	NP_001310009.1:p.Lys176=
NM_001323082.2:c.832A=	NP_001310011.1:p.Lys278=
NM_001323083.2:c.562A=	NP_001310012.1:p.Lys188=
NM_001323084.2:c.532A=	NP_001310013.1:p.Lys178=