Canonical Allele Identifier: CA376034158

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325745A>T (hg19) ; chr10:g.13283745A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283745A>T , CM000672.2:g.13283745A>T	GRCh38
NC_000010.10:g.13325745A>T , CM000672.1:g.13325745A>T	GRCh37
NC_000010.9:g.13365751A>T	NCBI36
NG_012862.1:g.21386T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.773T>A MANE Select	ENSP00000263038.4:p.Phe258Tyr
ENST00000263038.8:c.773T>A	ENSP00000263038.4:p.Phe258Tyr
ENST00000396913.6:c.473T>A	ENSP00000380121.2:p.Phe158Tyr
ENST00000396920.7:c.722T>A	ENSP00000380126.3:p.Phe241Tyr
ENST00000453759.6:c.473T>A	ENSP00000412525.2:p.Phe158Tyr
NM_001037537.1:c.473T>A	NP_001032626.1:p.Phe158Tyr
NM_006214.3:c.773T>A	NP_006205.1:p.Phe258Tyr
XM_005252469.2:c.554T>A	XP_005252526.1:p.Phe185Tyr
NM_001323080.1:c.473T>A	NP_001310009.1:p.Phe158Tyr
NM_001323082.1:c.779T>A	NP_001310011.1:p.Phe260Tyr
NM_001323083.1:c.509T>A	NP_001310012.1:p.Phe170Tyr
NM_001323084.1:c.479T>A	NP_001310013.1:p.Phe160Tyr
NM_006214.4:c.773T>A MANE Select	NP_006205.1:p.Phe258Tyr
NM_001037537.2:c.473T>A	NP_001032626.1:p.Phe158Tyr
NM_001323080.2:c.473T>A	NP_001310009.1:p.Phe158Tyr
NM_001323082.2:c.779T>A	NP_001310011.1:p.Phe260Tyr
NM_001323083.2:c.509T>A	NP_001310012.1:p.Phe170Tyr
NM_001323084.2:c.479T>A	NP_001310013.1:p.Phe160Tyr