Canonical Allele Identifier: CA1891546181

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283453G= , CM000672.2:g.13283453G=	GRCh38
NC_000010.10:g.13325453G= , CM000672.1:g.13325453G=	GRCh37
NC_000010.9:g.13365459G=	NCBI36
NG_012862.1:g.21678C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.828+237C= MANE Select	ENSP00000263038.4:n.828+237C=
ENST00000263038.8:c.828+237C=	ENSP00000263038.4:n.828+237C=
ENST00000396913.6:c.528+237C=	ENSP00000380121.2:n.528+237C=
ENST00000396920.7:c.777+237C=	ENSP00000380126.3:n.777+237C=
NM_001037537.1:c.528+237C=	NP_001032626.1:n.528+237C=
NM_006214.3:c.828+237C=	NP_006205.1:n.828+237C=
XM_005252469.2:c.609+237C=	XP_005252526.1:n.609+237C=
NM_001323080.1:c.528+237C=	NP_001310009.1:n.528+237C=
NM_001323082.1:c.834+237C=	NP_001310011.1:n.834+237C=
NM_001323083.1:c.564+237C=	NP_001310012.1:n.564+237C=
NM_001323084.1:c.534+237C=	NP_001310013.1:n.534+237C=
NM_006214.4:c.828+237C= MANE Select	NP_006205.1:n.828+237C=
NM_001037537.2:c.528+237C=	NP_001032626.1:n.528+237C=
NM_001323080.2:c.528+237C=	NP_001310009.1:n.528+237C=
NM_001323082.2:c.834+237C=	NP_001310011.1:n.834+237C=
NM_001323083.2:c.564+237C=	NP_001310012.1:n.564+237C=
NM_001323084.2:c.534+237C=	NP_001310013.1:n.534+237C=