Canonical Allele Identifier: CA1891546471

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283739G= , CM000672.2:g.13283739G=	GRCh38
NC_000010.10:g.13325739G= , CM000672.1:g.13325739G=	GRCh37
NC_000010.9:g.13365745G=	NCBI36
NG_012862.1:g.21392C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.779C= MANE Select	ENSP00000263038.4:p.Pro260=
ENST00000263038.8:c.779C=	ENSP00000263038.4:p.Pro260=
ENST00000396913.6:c.479C=	ENSP00000380121.2:p.Pro160=
ENST00000396920.7:c.728C=	ENSP00000380126.3:p.Pro243=
ENST00000453759.6:c.479C=	ENSP00000412525.2:p.Pro160=
NM_001037537.1:c.479C=	NP_001032626.1:p.Pro160=
NM_006214.3:c.779C=	NP_006205.1:p.Pro260=
XM_005252469.2:c.560C=	XP_005252526.1:p.Pro187=
NM_001323080.1:c.479C=	NP_001310009.1:p.Pro160=
NM_001323082.1:c.785C=	NP_001310011.1:p.Pro262=
NM_001323083.1:c.515C=	NP_001310012.1:p.Pro172=
NM_001323084.1:c.485C=	NP_001310013.1:p.Pro162=
NM_006214.4:c.779C= MANE Select	NP_006205.1:p.Pro260=
NM_001037537.2:c.479C=	NP_001032626.1:p.Pro160=
NM_001323080.2:c.479C=	NP_001310009.1:p.Pro160=
NM_001323082.2:c.785C=	NP_001310011.1:p.Pro262=
NM_001323083.2:c.515C=	NP_001310012.1:p.Pro172=
NM_001323084.2:c.485C=	NP_001310013.1:p.Pro162=