Canonical Allele Identifier: CA1891546491

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283754G= , CM000672.2:g.13283754G=	GRCh38
NC_000010.10:g.13325754G= , CM000672.1:g.13325754G=	GRCh37
NC_000010.9:g.13365760G=	NCBI36
NG_012862.1:g.21377C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.764C= MANE Select	ENSP00000263038.4:p.Thr255=
ENST00000263038.8:c.764C=	ENSP00000263038.4:p.Thr255=
ENST00000396913.6:c.464C=	ENSP00000380121.2:p.Thr155=
ENST00000396920.7:c.713C=	ENSP00000380126.3:p.Thr238=
ENST00000453759.6:c.464C=	ENSP00000412525.2:p.Thr155=
NM_001037537.1:c.464C=	NP_001032626.1:p.Thr155=
NM_006214.3:c.764C=	NP_006205.1:p.Thr255=
XM_005252469.2:c.545C=	XP_005252526.1:p.Thr182=
NM_001323080.1:c.464C=	NP_001310009.1:p.Thr155=
NM_001323082.1:c.770C=	NP_001310011.1:p.Thr257=
NM_001323083.1:c.500C=	NP_001310012.1:p.Thr167=
NM_001323084.1:c.470C=	NP_001310013.1:p.Thr157=
NM_006214.4:c.764C= MANE Select	NP_006205.1:p.Thr255=
NM_001037537.2:c.464C=	NP_001032626.1:p.Thr155=
NM_001323080.2:c.464C=	NP_001310009.1:p.Thr155=
NM_001323082.2:c.770C=	NP_001310011.1:p.Thr257=
NM_001323083.2:c.500C=	NP_001310012.1:p.Thr167=
NM_001323084.2:c.470C=	NP_001310013.1:p.Thr157=