Canonical Allele Identifier: CA1891546061

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13284077C= , CM000672.2:g.13284077C=	GRCh38
NC_000010.10:g.13326077C= , CM000672.1:g.13326077C=	GRCh37
NC_000010.9:g.13366083C=	NCBI36
NG_012862.1:g.21054G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.679-238G= MANE Select	ENSP00000263038.4:n.679-238G=
ENST00000263038.8:c.679-238G=	ENSP00000263038.4:n.679-238G=
ENST00000396913.6:c.379-238G=	ENSP00000380121.2:n.379-238G=
ENST00000396920.7:c.628-238G=	ENSP00000380126.3:n.628-238G=
ENST00000453759.6:c.379-238G=	ENSP00000412525.2:n.379-238G=
NM_001037537.1:c.379-238G=	NP_001032626.1:n.379-238G=
NM_006214.3:c.679-238G=	NP_006205.1:n.679-238G=
XM_005252469.2:c.460-238G=	XP_005252526.1:n.460-238G=
NM_001323080.1:c.379-238G=	NP_001310009.1:n.379-238G=
NM_001323082.1:c.685-238G=	NP_001310011.1:n.685-238G=
NM_001323083.1:c.415-238G=	NP_001310012.1:n.415-238G=
NM_001323084.1:c.385-238G=	NP_001310013.1:n.385-238G=
NM_006214.4:c.679-238G= MANE Select	NP_006205.1:n.679-238G=
NM_001037537.2:c.379-238G=	NP_001032626.1:n.379-238G=
NM_001323080.2:c.379-238G=	NP_001310009.1:n.379-238G=
NM_001323082.2:c.685-238G=	NP_001310011.1:n.685-238G=
NM_001323083.2:c.415-238G=	NP_001310012.1:n.415-238G=
NM_001323084.2:c.385-238G=	NP_001310013.1:n.385-238G=