Canonical Allele Identifier: CA376034196
Gene: PHYH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.13283762C>A , CM000672.2:g.13283762C>A GRCh38
NC_000010.10:g.13325762C>A , CM000672.1:g.13325762C>A GRCh37
NC_000010.9:g.13365768C>A NCBI36
NG_012862.1:g.21369G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263038.9:c.756G>T MANE Select ENSP00000263038.4:p.Lys252Asn
ENST00000263038.8:c.756G>T ENSP00000263038.4:p.Lys252Asn
ENST00000396913.6:c.456G>T ENSP00000380121.2:p.Lys152Asn
ENST00000396920.7:c.705G>T ENSP00000380126.3:p.Lys235Asn
ENST00000453759.6:c.456G>T ENSP00000412525.2:p.Lys152Asn
NM_001037537.1:c.456G>T NP_001032626.1:p.Lys152Asn
NM_006214.3:c.756G>T NP_006205.1:p.Lys252Asn
XM_005252469.2:c.537G>T XP_005252526.1:p.Lys179Asn
NM_001323080.1:c.456G>T NP_001310009.1:p.Lys152Asn
NM_001323082.1:c.762G>T NP_001310011.1:p.Lys254Asn
NM_001323083.1:c.492G>T NP_001310012.1:p.Lys164Asn
NM_001323084.1:c.462G>T NP_001310013.1:p.Lys154Asn
NM_006214.4:c.756G>T MANE Select NP_006205.1:p.Lys252Asn
NM_001037537.2:c.456G>T NP_001032626.1:p.Lys152Asn
NM_001323080.2:c.456G>T NP_001310009.1:p.Lys152Asn
NM_001323082.2:c.762G>T NP_001310011.1:p.Lys254Asn
NM_001323083.2:c.492G>T NP_001310012.1:p.Lys164Asn
NM_001323084.2:c.462G>T NP_001310013.1:p.Lys154Asn