Canonical Allele Identifier: CA1891548436
Gene: PHYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.13288437G= , CM000672.2:g.13288437G= GRCh38
NC_000010.10:g.13330437G= , CM000672.1:g.13330437G= GRCh37
NC_000010.9:g.13370443G= NCBI36
NG_012862.1:g.16694C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263038.9:c.601C= MANE Select ENSP00000263038.4:p.Arg201=
ENST00000263038.8:c.601C= ENSP00000263038.4:p.Arg201=
ENST00000396913.6:c.301C= ENSP00000380121.2:p.Arg101=
ENST00000396920.7:c.550C= ENSP00000380126.3:p.Arg184=
ENST00000453759.6:c.301C= ENSP00000412525.2:p.Arg101=
ENST00000479604.1:c.607C= ENSP00000420117.1:p.Arg203=
NM_001037537.1:c.301C= NP_001032626.1:p.Arg101=
NM_006214.3:c.601C= NP_006205.1:p.Arg201=
XM_005252469.2:c.460-4598C= XP_005252526.1:n.460-4598C=
NM_001323080.1:c.301C= NP_001310009.1:p.Arg101=
NM_001323082.1:c.607C= NP_001310011.1:p.Arg203=
NM_001323083.1:c.415-4598C= NP_001310012.1:n.415-4598C=
NM_001323084.1:c.307C= NP_001310013.1:p.Arg103=
NM_006214.4:c.601C= MANE Select NP_006205.1:p.Arg201=
NM_001037537.2:c.301C= NP_001032626.1:p.Arg101=
NM_001323080.2:c.301C= NP_001310009.1:p.Arg101=
NM_001323082.2:c.607C= NP_001310011.1:p.Arg203=
NM_001323083.2:c.415-4598C= NP_001310012.1:n.415-4598C=
NM_001323084.2:c.307C= NP_001310013.1:p.Arg103=