Canonical Allele Identifier: CA376034126

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325731T>A (hg19) ; chr10:g.13283731T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283731T>A , CM000672.2:g.13283731T>A	GRCh38
NC_000010.10:g.13325731T>A , CM000672.1:g.13325731T>A	GRCh37
NC_000010.9:g.13365737T>A	NCBI36
NG_012862.1:g.21400A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.787A>T MANE Select	ENSP00000263038.4:p.Ile263Phe
ENST00000263038.8:c.787A>T	ENSP00000263038.4:p.Ile263Phe
ENST00000396913.6:c.487A>T	ENSP00000380121.2:p.Ile163Phe
ENST00000396920.7:c.736A>T	ENSP00000380126.3:p.Ile246Phe
ENST00000453759.6:c.487A>T	ENSP00000412525.2:p.Ile163Phe
NM_001037537.1:c.487A>T	NP_001032626.1:p.Ile163Phe
NM_006214.3:c.787A>T	NP_006205.1:p.Ile263Phe
XM_005252469.2:c.568A>T	XP_005252526.1:p.Ile190Phe
NM_001323080.1:c.487A>T	NP_001310009.1:p.Ile163Phe
NM_001323082.1:c.793A>T	NP_001310011.1:p.Ile265Phe
NM_001323083.1:c.523A>T	NP_001310012.1:p.Ile175Phe
NM_001323084.1:c.493A>T	NP_001310013.1:p.Ile165Phe
NM_006214.4:c.787A>T MANE Select	NP_006205.1:p.Ile263Phe
NM_001037537.2:c.487A>T	NP_001032626.1:p.Ile163Phe
NM_001323080.2:c.487A>T	NP_001310009.1:p.Ile163Phe
NM_001323082.2:c.793A>T	NP_001310011.1:p.Ile265Phe
NM_001323083.2:c.523A>T	NP_001310012.1:p.Ile175Phe
NM_001323084.2:c.493A>T	NP_001310013.1:p.Ile165Phe