Canonical Allele Identifier: CA2786697221

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283667_13283675del , CM000672.2:g.13283667_13283675del	GRCh38
NC_000010.10:g.13325667_13325675del , CM000672.1:g.13325667_13325675del	GRCh37
NC_000010.9:g.13365673_13365681del	NCBI36
NG_012862.1:g.21463_21471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.828+22_828+30del MANE Select	ENSP00000263038.4:n.828+22_828+30del
ENST00000263038.8:c.828+22_828+30del	ENSP00000263038.4:n.828+22_828+30del
ENST00000396913.6:c.528+22_528+30del	ENSP00000380121.2:n.528+22_528+30del
ENST00000396920.7:c.777+22_777+30del	ENSP00000380126.3:n.777+22_777+30del
NM_001037537.1:c.528+22_528+30del	NP_001032626.1:n.528+22_528+30del
NM_006214.3:c.828+22_828+30del	NP_006205.1:n.828+22_828+30del
XM_005252469.2:c.609+22_609+30del	XP_005252526.1:n.609+22_609+30del
NM_001323080.1:c.528+22_528+30del	NP_001310009.1:n.528+22_528+30del
NM_001323082.1:c.834+22_834+30del	NP_001310011.1:n.834+22_834+30del
NM_001323083.1:c.564+22_564+30del	NP_001310012.1:n.564+22_564+30del
NM_001323084.1:c.534+22_534+30del	NP_001310013.1:n.534+22_534+30del
NM_006214.4:c.828+22_828+30del MANE Select	NP_006205.1:n.828+22_828+30del
NM_001037537.2:c.528+22_528+30del	NP_001032626.1:n.528+22_528+30del
NM_001323080.2:c.528+22_528+30del	NP_001310009.1:n.528+22_528+30del
NM_001323082.2:c.834+22_834+30del	NP_001310011.1:n.834+22_834+30del
NM_001323083.2:c.564+22_564+30del	NP_001310012.1:n.564+22_564+30del
NM_001323084.2:c.534+22_534+30del	NP_001310013.1:n.534+22_534+30del