Canonical Allele Identifier: CA1891546516

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283772A= , CM000672.2:g.13283772A=	GRCh38
NC_000010.10:g.13325772A= , CM000672.1:g.13325772A=	GRCh37
NC_000010.9:g.13365778A=	NCBI36
NG_012862.1:g.21359T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.746T= MANE Select	ENSP00000263038.4:p.Val249=
ENST00000263038.8:c.746T=	ENSP00000263038.4:p.Val249=
ENST00000396913.6:c.446T=	ENSP00000380121.2:p.Val149=
ENST00000396920.7:c.695T=	ENSP00000380126.3:p.Val232=
ENST00000453759.6:c.446T=	ENSP00000412525.2:p.Val149=
NM_001037537.1:c.446T=	NP_001032626.1:p.Val149=
NM_006214.3:c.746T=	NP_006205.1:p.Val249=
XM_005252469.2:c.527T=	XP_005252526.1:p.Val176=
NM_001323080.1:c.446T=	NP_001310009.1:p.Val149=
NM_001323082.1:c.752T=	NP_001310011.1:p.Val251=
NM_001323083.1:c.482T=	NP_001310012.1:p.Val161=
NM_001323084.1:c.452T=	NP_001310013.1:p.Val151=
NM_006214.4:c.746T= MANE Select	NP_006205.1:p.Val249=
NM_001037537.2:c.446T=	NP_001032626.1:p.Val149=
NM_001323080.2:c.446T=	NP_001310009.1:p.Val149=
NM_001323082.2:c.752T=	NP_001310011.1:p.Val251=
NM_001323083.2:c.482T=	NP_001310012.1:p.Val161=
NM_001323084.2:c.452T=	NP_001310013.1:p.Val151=