Canonical Allele Identifier: CA376034105

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325721G>T (hg19) ; chr10:g.13283721G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283721G>T , CM000672.2:g.13283721G>T	GRCh38
NC_000010.10:g.13325721G>T , CM000672.1:g.13325721G>T	GRCh37
NC_000010.9:g.13365727G>T	NCBI36
NG_012862.1:g.21410C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.797C>A MANE Select	ENSP00000263038.4:p.Ser266Tyr
ENST00000263038.8:c.797C>A	ENSP00000263038.4:p.Ser266Tyr
ENST00000396913.6:c.497C>A	ENSP00000380121.2:p.Ser166Tyr
ENST00000396920.7:c.746C>A	ENSP00000380126.3:p.Ser249Tyr
ENST00000453759.6:c.497C>A	ENSP00000412525.2:p.Ser166Tyr
NM_001037537.1:c.497C>A	NP_001032626.1:p.Ser166Tyr
NM_006214.3:c.797C>A	NP_006205.1:p.Ser266Tyr
XM_005252469.2:c.578C>A	XP_005252526.1:p.Ser193Tyr
NM_001323080.1:c.497C>A	NP_001310009.1:p.Ser166Tyr
NM_001323082.1:c.803C>A	NP_001310011.1:p.Ser268Tyr
NM_001323083.1:c.533C>A	NP_001310012.1:p.Ser178Tyr
NM_001323084.1:c.503C>A	NP_001310013.1:p.Ser168Tyr
NM_006214.4:c.797C>A MANE Select	NP_006205.1:p.Ser266Tyr
NM_001037537.2:c.497C>A	NP_001032626.1:p.Ser166Tyr
NM_001323080.2:c.497C>A	NP_001310009.1:p.Ser166Tyr
NM_001323082.2:c.803C>A	NP_001310011.1:p.Ser268Tyr
NM_001323083.2:c.533C>A	NP_001310012.1:p.Ser178Tyr
NM_001323084.2:c.503C>A	NP_001310013.1:p.Ser168Tyr