Canonical Allele Identifier: CA1891546413

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283706G= , CM000672.2:g.13283706G=	GRCh38
NC_000010.10:g.13325706G= , CM000672.1:g.13325706G=	GRCh37
NC_000010.9:g.13365712G=	NCBI36
NG_012862.1:g.21425C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263038.9:c.812C= MANE Select	ENSP00000263038.4:p.Thr271=
ENST00000263038.8:c.812C=	ENSP00000263038.4:p.Thr271=
ENST00000396913.6:c.512C=	ENSP00000380121.2:p.Thr171=
ENST00000396920.7:c.761C=	ENSP00000380126.3:p.Thr254=
ENST00000453759.6:c.512C=	ENSP00000412525.2:p.Thr171=
NM_001037537.1:c.512C=	NP_001032626.1:p.Thr171=
NM_006214.3:c.812C=	NP_006205.1:p.Thr271=
XM_005252469.2:c.593C=	XP_005252526.1:p.Thr198=
NM_001323080.1:c.512C=	NP_001310009.1:p.Thr171=
NM_001323082.1:c.818C=	NP_001310011.1:p.Thr273=
NM_001323083.1:c.548C=	NP_001310012.1:p.Thr183=
NM_001323084.1:c.518C=	NP_001310013.1:p.Thr173=
NM_006214.4:c.812C= MANE Select	NP_006205.1:p.Thr271=
NM_001037537.2:c.512C=	NP_001032626.1:p.Thr171=
NM_001323080.2:c.512C=	NP_001310009.1:p.Thr171=
NM_001323082.2:c.818C=	NP_001310011.1:p.Thr273=
NM_001323083.2:c.548C=	NP_001310012.1:p.Thr183=
NM_001323084.2:c.518C=	NP_001310013.1:p.Thr173=