Canonical Allele Identifier: CA2786697281

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283943_13283944insAGAG , CM000672.2:g.13283943_13283944insAGAG	GRCh38
NC_000010.10:g.13325943_13325944insAGAG , CM000672.1:g.13325943_13325944insAGAG	GRCh37
NC_000010.9:g.13365949_13365950insAGAG	NCBI36
NG_012862.1:g.21187_21188insCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.679-105_679-104insCTCT MANE Select	ENSP00000263038.4:n.679-105_679-104insCTCT
ENST00000263038.8:c.679-105_679-104insCTCT	ENSP00000263038.4:n.679-105_679-104insCTCT
ENST00000396913.6:c.379-105_379-104insCTCT	ENSP00000380121.2:n.379-105_379-104insCTCT
ENST00000396920.7:c.628-105_628-104insCTCT	ENSP00000380126.3:n.628-105_628-104insCTCT
ENST00000453759.6:c.379-105_379-104insCTCT	ENSP00000412525.2:n.379-105_379-104insCTCT
NM_001037537.1:c.379-105_379-104insCTCT	NP_001032626.1:n.379-105_379-104insCTCT
NM_006214.3:c.679-105_679-104insCTCT	NP_006205.1:n.679-105_679-104insCTCT
XM_005252469.2:c.460-105_460-104insCTCT	XP_005252526.1:n.460-105_460-104insCTCT
NM_001323080.1:c.379-105_379-104insCTCT	NP_001310009.1:n.379-105_379-104insCTCT
NM_001323082.1:c.685-105_685-104insCTCT	NP_001310011.1:n.685-105_685-104insCTCT
NM_001323083.1:c.415-105_415-104insCTCT	NP_001310012.1:n.415-105_415-104insCTCT
NM_001323084.1:c.385-105_385-104insCTCT	NP_001310013.1:n.385-105_385-104insCTCT
NM_006214.4:c.679-105_679-104insCTCT MANE Select	NP_006205.1:n.679-105_679-104insCTCT
NM_001037537.2:c.379-105_379-104insCTCT	NP_001032626.1:n.379-105_379-104insCTCT
NM_001323080.2:c.379-105_379-104insCTCT	NP_001310009.1:n.379-105_379-104insCTCT
NM_001323082.2:c.685-105_685-104insCTCT	NP_001310011.1:n.685-105_685-104insCTCT
NM_001323083.2:c.415-105_415-104insCTCT	NP_001310012.1:n.415-105_415-104insCTCT
NM_001323084.2:c.385-105_385-104insCTCT	NP_001310013.1:n.385-105_385-104insCTCT