Canonical Allele Identifier: CA1891553355
Gene: PHYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.13298220A= , CM000672.2:g.13298220A= GRCh38
NC_000010.10:g.13340220A= , CM000672.1:g.13340220A= GRCh37
NC_000010.9:g.13380226A= NCBI36
NG_012862.1:g.6911T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263038.9:c.101T= MANE Select ENSP00000263038.4:p.Ile34=
ENST00000263038.8:c.101T= ENSP00000263038.4:p.Ile34=
ENST00000396913.6:c.-167+1200T= ENSP00000380121.2:n.-167+1200T=
ENST00000396920.7:c.44T= ENSP00000380126.3:p.Ile15=
ENST00000453759.6:c.-200T= ENSP00000412525.2:n.-200T=
ENST00000463730.1:n.156T=
ENST00000479604.1:c.101T= ENSP00000420117.1:p.Ile34=
NM_001037537.1:c.-167+1200T= NP_001032626.1:n.-167+1200T=
NM_006214.3:c.101T= NP_006205.1:p.Ile34=
XM_005252469.2:c.146T= XP_005252526.1:p.Ile49=
NM_001323080.1:c.-200T= NP_001310009.1:n.-200T=
NM_001323082.1:c.101T= NP_001310011.1:p.Ile34=
NM_001323083.1:c.101T= NP_001310012.1:p.Ile34=
NM_001323084.1:c.-167+1200T= NP_001310013.1:n.-167+1200T=
NM_006214.4:c.101T= MANE Select NP_006205.1:p.Ile34=
NM_001037537.2:c.-167+1200T= NP_001032626.1:n.-167+1200T=
NM_001323080.2:c.-200T= NP_001310009.1:n.-200T=
NM_001323082.2:c.101T= NP_001310011.1:p.Ile34=
NM_001323083.2:c.101T= NP_001310012.1:p.Ile34=
NM_001323084.2:c.-167+1200T= NP_001310013.1:n.-167+1200T=