Canonical Allele Identifier: CA1891546324
Gene: PHYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.13283637T= , CM000672.2:g.13283637T= GRCh38
NC_000010.10:g.13325637T= , CM000672.1:g.13325637T= GRCh37
NC_000010.9:g.13365643T= NCBI36
NG_012862.1:g.21494A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263038.9:c.828+53A= MANE Select ENSP00000263038.4:n.828+53A=
ENST00000263038.8:c.828+53A= ENSP00000263038.4:n.828+53A=
ENST00000396913.6:c.528+53A= ENSP00000380121.2:n.528+53A=
ENST00000396920.7:c.777+53A= ENSP00000380126.3:n.777+53A=
NM_001037537.1:c.528+53A= NP_001032626.1:n.528+53A=
NM_006214.3:c.828+53A= NP_006205.1:n.828+53A=
XM_005252469.2:c.609+53A= XP_005252526.1:n.609+53A=
NM_001323080.1:c.528+53A= NP_001310009.1:n.528+53A=
NM_001323082.1:c.834+53A= NP_001310011.1:n.834+53A=
NM_001323083.1:c.564+53A= NP_001310012.1:n.564+53A=
NM_001323084.1:c.534+53A= NP_001310013.1:n.534+53A=
NM_006214.4:c.828+53A= MANE Select NP_006205.1:n.828+53A=
NM_001037537.2:c.528+53A= NP_001032626.1:n.528+53A=
NM_001323080.2:c.528+53A= NP_001310009.1:n.528+53A=
NM_001323082.2:c.834+53A= NP_001310011.1:n.834+53A=
NM_001323083.2:c.564+53A= NP_001310012.1:n.564+53A=
NM_001323084.2:c.534+53A= NP_001310013.1:n.534+53A=