Canonical Allele Identifier: CA1891546540

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283783C= , CM000672.2:g.13283783C=	GRCh38
NC_000010.10:g.13325783C= , CM000672.1:g.13325783C=	GRCh37
NC_000010.9:g.13365789C=	NCBI36
NG_012862.1:g.21348G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.735G= MANE Select	ENSP00000263038.4:p.Arg245=
ENST00000263038.8:c.735G=	ENSP00000263038.4:p.Arg245=
ENST00000396913.6:c.435G=	ENSP00000380121.2:p.Arg145=
ENST00000396920.7:c.684G=	ENSP00000380126.3:p.Arg228=
ENST00000453759.6:c.435G=	ENSP00000412525.2:p.Arg145=
NM_001037537.1:c.435G=	NP_001032626.1:p.Arg145=
NM_006214.3:c.735G=	NP_006205.1:p.Arg245=
XM_005252469.2:c.516G=	XP_005252526.1:p.Arg172=
NM_001323080.1:c.435G=	NP_001310009.1:p.Arg145=
NM_001323082.1:c.741G=	NP_001310011.1:p.Arg247=
NM_001323083.1:c.471G=	NP_001310012.1:p.Arg157=
NM_001323084.1:c.441G=	NP_001310013.1:p.Arg147=
NM_006214.4:c.735G= MANE Select	NP_006205.1:p.Arg245=
NM_001037537.2:c.435G=	NP_001032626.1:p.Arg145=
NM_001323080.2:c.435G=	NP_001310009.1:p.Arg145=
NM_001323082.2:c.741G=	NP_001310011.1:p.Arg247=
NM_001323083.2:c.471G=	NP_001310012.1:p.Arg157=
NM_001323084.2:c.441G=	NP_001310013.1:p.Arg147=