Canonical Allele Identifier: CA468242036

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13340219A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13298219A>T , CM000672.2:g.13298219A>T	GRCh38
NC_000010.10:g.13340219A>T , CM000672.1:g.13340219A>T	GRCh37
NC_000010.9:g.13380225A>T	NCBI36
NG_012862.1:g.6912T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263038.9:c.102T>A MANE Select	ENSP00000263038.4:p.Ile34=
ENST00000263038.8:c.102T>A	ENSP00000263038.4:p.Ile34=
ENST00000396913.6:c.-167+1201T>A	ENSP00000380121.2:n.-167+1201T>A
ENST00000396920.7:c.45T>A	ENSP00000380126.3:p.Ile15=
ENST00000453759.6:c.-199T>A	ENSP00000412525.2:n.-199T>A
ENST00000463730.1:n.157T>A
ENST00000479604.1:c.102T>A	ENSP00000420117.1:p.Ile34=
NM_001037537.1:c.-167+1201T>A	NP_001032626.1:n.-167+1201T>A
NM_006214.3:c.102T>A	NP_006205.1:p.Ile34=
XM_005252469.2:c.147T>A	XP_005252526.1:p.Ile49=
NM_001323080.1:c.-199T>A	NP_001310009.1:n.-199T>A
NM_001323082.1:c.102T>A	NP_001310011.1:p.Ile34=
NM_001323083.1:c.102T>A	NP_001310012.1:p.Ile34=
NM_001323084.1:c.-167+1201T>A	NP_001310013.1:n.-167+1201T>A
NM_006214.4:c.102T>A MANE Select	NP_006205.1:p.Ile34=
NM_001037537.2:c.-167+1201T>A	NP_001032626.1:n.-167+1201T>A
NM_001323080.2:c.-199T>A	NP_001310009.1:n.-199T>A
NM_001323082.2:c.102T>A	NP_001310011.1:p.Ile34=
NM_001323083.2:c.102T>A	NP_001310012.1:p.Ile34=
NM_001323084.2:c.-167+1201T>A	NP_001310013.1:n.-167+1201T>A