Canonical Allele Identifier: CA1891546485

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283750_13283752delinsAAC , CM000672.2:g.13283750_13283752delinsAAC	GRCh38
NC_000010.10:g.13325750_13325752delinsAAC , CM000672.1:g.13325750_13325752delinsAAC	GRCh37
NC_000010.9:g.13365756_13365758delinsAAC	NCBI36
NG_012862.1:g.21379_21381delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.766_768delinsGTT MANE Select	ENSP00000263038.4:p.Val256=
ENST00000263038.8:c.766_768delinsGTT	ENSP00000263038.4:p.Val256=
ENST00000396913.6:c.466_468delinsGTT	ENSP00000380121.2:p.Val156=
ENST00000396920.7:c.715_717delinsGTT	ENSP00000380126.3:p.Val239=
ENST00000453759.6:c.466_468delinsGTT	ENSP00000412525.2:p.Val156=
NM_001037537.1:c.466_468delinsGTT	NP_001032626.1:p.Val156=
NM_006214.3:c.766_768delinsGTT	NP_006205.1:p.Val256=
XM_005252469.2:c.547_549delinsGTT	XP_005252526.1:p.Val183=
NM_001323080.1:c.466_468delinsGTT	NP_001310009.1:p.Val156=
NM_001323082.1:c.772_774delinsGTT	NP_001310011.1:p.Val258=
NM_001323083.1:c.502_504delinsGTT	NP_001310012.1:p.Val168=
NM_001323084.1:c.472_474delinsGTT	NP_001310013.1:p.Val158=
NM_006214.4:c.766_768delinsGTT MANE Select	NP_006205.1:p.Val256=
NM_001037537.2:c.466_468delinsGTT	NP_001032626.1:p.Val156=
NM_001323080.2:c.466_468delinsGTT	NP_001310009.1:p.Val156=
NM_001323082.2:c.772_774delinsGTT	NP_001310011.1:p.Val258=
NM_001323083.2:c.502_504delinsGTT	NP_001310012.1:p.Val168=
NM_001323084.2:c.472_474delinsGTT	NP_001310013.1:p.Val158=