Canonical Allele Identifier: CA1891546476

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283744G= , CM000672.2:g.13283744G=	GRCh38
NC_000010.10:g.13325744G= , CM000672.1:g.13325744G=	GRCh37
NC_000010.9:g.13365750G=	NCBI36
NG_012862.1:g.21387C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.774C= MANE Select	ENSP00000263038.4:p.Phe258=
ENST00000263038.8:c.774C=	ENSP00000263038.4:p.Phe258=
ENST00000396913.6:c.474C=	ENSP00000380121.2:p.Phe158=
ENST00000396920.7:c.723C=	ENSP00000380126.3:p.Phe241=
ENST00000453759.6:c.474C=	ENSP00000412525.2:p.Phe158=
NM_001037537.1:c.474C=	NP_001032626.1:p.Phe158=
NM_006214.3:c.774C=	NP_006205.1:p.Phe258=
XM_005252469.2:c.555C=	XP_005252526.1:p.Phe185=
NM_001323080.1:c.474C=	NP_001310009.1:p.Phe158=
NM_001323082.1:c.780C=	NP_001310011.1:p.Phe260=
NM_001323083.1:c.510C=	NP_001310012.1:p.Phe170=
NM_001323084.1:c.480C=	NP_001310013.1:p.Phe160=
NM_006214.4:c.774C= MANE Select	NP_006205.1:p.Phe258=
NM_001037537.2:c.474C=	NP_001032626.1:p.Phe158=
NM_001323080.2:c.474C=	NP_001310009.1:p.Phe158=
NM_001323082.2:c.780C=	NP_001310011.1:p.Phe260=
NM_001323083.2:c.510C=	NP_001310012.1:p.Phe170=
NM_001323084.2:c.480C=	NP_001310013.1:p.Phe160=