Canonical Allele Identifier: CA468237073

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325785G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283785G>T , CM000672.2:g.13283785G>T	GRCh38
NC_000010.10:g.13325785G>T , CM000672.1:g.13325785G>T	GRCh37
NC_000010.9:g.13365791G>T	NCBI36
NG_012862.1:g.21346C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.733C>A MANE Select	ENSP00000263038.4:p.Arg245=
ENST00000263038.8:c.733C>A	ENSP00000263038.4:p.Arg245=
ENST00000396913.6:c.433C>A	ENSP00000380121.2:p.Arg145=
ENST00000396920.7:c.682C>A	ENSP00000380126.3:p.Arg228=
ENST00000453759.6:c.433C>A	ENSP00000412525.2:p.Arg145=
NM_001037537.1:c.433C>A	NP_001032626.1:p.Arg145=
NM_006214.3:c.733C>A	NP_006205.1:p.Arg245=
XM_005252469.2:c.514C>A	XP_005252526.1:p.Arg172=
NM_001323080.1:c.433C>A	NP_001310009.1:p.Arg145=
NM_001323082.1:c.739C>A	NP_001310011.1:p.Arg247=
NM_001323083.1:c.469C>A	NP_001310012.1:p.Arg157=
NM_001323084.1:c.439C>A	NP_001310013.1:p.Arg147=
NM_006214.4:c.733C>A MANE Select	NP_006205.1:p.Arg245=
NM_001037537.2:c.433C>A	NP_001032626.1:p.Arg145=
NM_001323080.2:c.433C>A	NP_001310009.1:p.Arg145=
NM_001323082.2:c.739C>A	NP_001310011.1:p.Arg247=
NM_001323083.2:c.469C>A	NP_001310012.1:p.Arg157=
NM_001323084.2:c.439C>A	NP_001310013.1:p.Arg147=