Canonical Allele Identifier: CA1891546880

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13284004_13284005delinsAG , CM000672.2:g.13284004_13284005delinsAG	GRCh38
NC_000010.10:g.13326004_13326005delinsAG , CM000672.1:g.13326004_13326005delinsAG	GRCh37
NC_000010.9:g.13366010_13366011delinsAG	NCBI36
NG_012862.1:g.21126_21127delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.679-166_679-165delinsCT MANE Select	ENSP00000263038.4:n.679-166_679-165delinsCT
ENST00000263038.8:c.679-166_679-165delinsCT	ENSP00000263038.4:n.679-166_679-165delinsCT
ENST00000396913.6:c.379-166_379-165delinsCT	ENSP00000380121.2:n.379-166_379-165delinsCT
ENST00000396920.7:c.628-166_628-165delinsCT	ENSP00000380126.3:n.628-166_628-165delinsCT
ENST00000453759.6:c.379-166_379-165delinsCT	ENSP00000412525.2:n.379-166_379-165delinsCT
NM_001037537.1:c.379-166_379-165delinsCT	NP_001032626.1:n.379-166_379-165delinsCT
NM_006214.3:c.679-166_679-165delinsCT	NP_006205.1:n.679-166_679-165delinsCT
XM_005252469.2:c.460-166_460-165delinsCT	XP_005252526.1:n.460-166_460-165delinsCT
NM_001323080.1:c.379-166_379-165delinsCT	NP_001310009.1:n.379-166_379-165delinsCT
NM_001323082.1:c.685-166_685-165delinsCT	NP_001310011.1:n.685-166_685-165delinsCT
NM_001323083.1:c.415-166_415-165delinsCT	NP_001310012.1:n.415-166_415-165delinsCT
NM_001323084.1:c.385-166_385-165delinsCT	NP_001310013.1:n.385-166_385-165delinsCT
NM_006214.4:c.679-166_679-165delinsCT MANE Select	NP_006205.1:n.679-166_679-165delinsCT
NM_001037537.2:c.379-166_379-165delinsCT	NP_001032626.1:n.379-166_379-165delinsCT
NM_001323080.2:c.379-166_379-165delinsCT	NP_001310009.1:n.379-166_379-165delinsCT
NM_001323082.2:c.685-166_685-165delinsCT	NP_001310011.1:n.685-166_685-165delinsCT
NM_001323083.2:c.415-166_415-165delinsCT	NP_001310012.1:n.415-166_415-165delinsCT
NM_001323084.2:c.385-166_385-165delinsCT	NP_001310013.1:n.385-166_385-165delinsCT