Canonical Allele Identifier: CA2608290904

Gene: PHYH

Linked Data

• dbSNP Id: rs2131660883
• gnomAD v4: 10-13298124-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13298126del , CM000672.2:g.13298126del	GRCh38
NC_000010.10:g.13340126del , CM000672.1:g.13340126del	GRCh37
NC_000010.9:g.13380132del	NCBI36
NG_012862.1:g.7006del

Transcript Alleles

HGVS	Amino-acid change
ENST00000263038.9:c.134+62del MANE Select	ENSP00000263038.4:n.134+62del
ENST00000263038.8:c.134+62del	ENSP00000263038.4:n.134+62del
ENST00000396913.6:c.-167+1295del	ENSP00000380121.2:n.-167+1295del
ENST00000396920.7:c.77+62del	ENSP00000380126.3:n.77+62del
ENST00000453759.6:c.-167+62del	ENSP00000412525.2:n.-167+62del
ENST00000463730.1:n.189+62del
ENST00000479604.1:c.134+62del	ENSP00000420117.1:n.134+62del
NM_001037537.1:c.-167+1295del	NP_001032626.1:n.-167+1295del
NM_006214.3:c.134+62del	NP_006205.1:n.134+62del
XM_005252469.2:c.179+62del	XP_005252526.1:n.179+62del
NM_001323080.1:c.-167+62del	NP_001310009.1:n.-167+62del
NM_001323082.1:c.134+62del	NP_001310011.1:n.134+62del
NM_001323083.1:c.134+62del	NP_001310012.1:n.134+62del
NM_001323084.1:c.-167+1295del	NP_001310013.1:n.-167+1295del
NM_006214.4:c.134+62del MANE Select	NP_006205.1:n.134+62del
NM_001037537.2:c.-167+1295del	NP_001032626.1:n.-167+1295del
NM_001323080.2:c.-167+62del	NP_001310009.1:n.-167+62del
NM_001323082.2:c.134+62del	NP_001310011.1:n.134+62del
NM_001323083.2:c.134+62del	NP_001310012.1:n.134+62del
NM_001323084.2:c.-167+1295del	NP_001310013.1:n.-167+1295del