Canonical Allele Identifier: CA468236855

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325723T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283723T>C , CM000672.2:g.13283723T>C	GRCh38
NC_000010.10:g.13325723T>C , CM000672.1:g.13325723T>C	GRCh37
NC_000010.9:g.13365729T>C	NCBI36
NG_012862.1:g.21408A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.795A>G MANE Select	ENSP00000263038.4:p.Gly265=
ENST00000263038.8:c.795A>G	ENSP00000263038.4:p.Gly265=
ENST00000396913.6:c.495A>G	ENSP00000380121.2:p.Gly165=
ENST00000396920.7:c.744A>G	ENSP00000380126.3:p.Gly248=
ENST00000453759.6:c.495A>G	ENSP00000412525.2:p.Gly165=
NM_001037537.1:c.495A>G	NP_001032626.1:p.Gly165=
NM_006214.3:c.795A>G	NP_006205.1:p.Gly265=
XM_005252469.2:c.576A>G	XP_005252526.1:p.Gly192=
NM_001323080.1:c.495A>G	NP_001310009.1:p.Gly165=
NM_001323082.1:c.801A>G	NP_001310011.1:p.Gly267=
NM_001323083.1:c.531A>G	NP_001310012.1:p.Gly177=
NM_001323084.1:c.501A>G	NP_001310013.1:p.Gly167=
NM_006214.4:c.795A>G MANE Select	NP_006205.1:p.Gly265=
NM_001037537.2:c.495A>G	NP_001032626.1:p.Gly165=
NM_001323080.2:c.495A>G	NP_001310009.1:p.Gly165=
NM_001323082.2:c.801A>G	NP_001310011.1:p.Gly267=
NM_001323083.2:c.531A>G	NP_001310012.1:p.Gly177=
NM_001323084.2:c.501A>G	NP_001310013.1:p.Gly167=