Canonical Allele Identifier: CA1891548433
Gene: PHYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.13288433T= , CM000672.2:g.13288433T= GRCh38
NC_000010.10:g.13330433T= , CM000672.1:g.13330433T= GRCh37
NC_000010.9:g.13370439T= NCBI36
NG_012862.1:g.16698A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263038.9:c.605A= MANE Select ENSP00000263038.4:p.Asn202=
ENST00000263038.8:c.605A= ENSP00000263038.4:p.Asn202=
ENST00000396913.6:c.305A= ENSP00000380121.2:p.Asn102=
ENST00000396920.7:c.554A= ENSP00000380126.3:p.Asn185=
ENST00000453759.6:c.305A= ENSP00000412525.2:p.Asn102=
ENST00000479604.1:c.611A= ENSP00000420117.1:p.Asn204=
NM_001037537.1:c.305A= NP_001032626.1:p.Asn102=
NM_006214.3:c.605A= NP_006205.1:p.Asn202=
XM_005252469.2:c.460-4594A= XP_005252526.1:n.460-4594A=
NM_001323080.1:c.305A= NP_001310009.1:p.Asn102=
NM_001323082.1:c.611A= NP_001310011.1:p.Asn204=
NM_001323083.1:c.415-4594A= NP_001310012.1:n.415-4594A=
NM_001323084.1:c.311A= NP_001310013.1:p.Asn104=
NM_006214.4:c.605A= MANE Select NP_006205.1:p.Asn202=
NM_001037537.2:c.305A= NP_001032626.1:p.Asn102=
NM_001323080.2:c.305A= NP_001310009.1:p.Asn102=
NM_001323082.2:c.611A= NP_001310011.1:p.Asn204=
NM_001323083.2:c.415-4594A= NP_001310012.1:n.415-4594A=
NM_001323084.2:c.311A= NP_001310013.1:p.Asn104=