Canonical Allele Identifier: CA1891546858

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283984_13283985delinsCA , CM000672.2:g.13283984_13283985delinsCA	GRCh38
NC_000010.10:g.13325984_13325985delinsCA , CM000672.1:g.13325984_13325985delinsCA	GRCh37
NC_000010.9:g.13365990_13365991delinsCA	NCBI36
NG_012862.1:g.21146_21147delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.679-146_679-145delinsTG MANE Select	ENSP00000263038.4:n.679-146_679-145delinsTG
ENST00000263038.8:c.679-146_679-145delinsTG	ENSP00000263038.4:n.679-146_679-145delinsTG
ENST00000396913.6:c.379-146_379-145delinsTG	ENSP00000380121.2:n.379-146_379-145delinsTG
ENST00000396920.7:c.628-146_628-145delinsTG	ENSP00000380126.3:n.628-146_628-145delinsTG
ENST00000453759.6:c.379-146_379-145delinsTG	ENSP00000412525.2:n.379-146_379-145delinsTG
NM_001037537.1:c.379-146_379-145delinsTG	NP_001032626.1:n.379-146_379-145delinsTG
NM_006214.3:c.679-146_679-145delinsTG	NP_006205.1:n.679-146_679-145delinsTG
XM_005252469.2:c.460-146_460-145delinsTG	XP_005252526.1:n.460-146_460-145delinsTG
NM_001323080.1:c.379-146_379-145delinsTG	NP_001310009.1:n.379-146_379-145delinsTG
NM_001323082.1:c.685-146_685-145delinsTG	NP_001310011.1:n.685-146_685-145delinsTG
NM_001323083.1:c.415-146_415-145delinsTG	NP_001310012.1:n.415-146_415-145delinsTG
NM_001323084.1:c.385-146_385-145delinsTG	NP_001310013.1:n.385-146_385-145delinsTG
NM_006214.4:c.679-146_679-145delinsTG MANE Select	NP_006205.1:n.679-146_679-145delinsTG
NM_001037537.2:c.379-146_379-145delinsTG	NP_001032626.1:n.379-146_379-145delinsTG
NM_001323080.2:c.379-146_379-145delinsTG	NP_001310009.1:n.379-146_379-145delinsTG
NM_001323082.2:c.685-146_685-145delinsTG	NP_001310011.1:n.685-146_685-145delinsTG
NM_001323083.2:c.415-146_415-145delinsTG	NP_001310012.1:n.415-146_415-145delinsTG
NM_001323084.2:c.385-146_385-145delinsTG	NP_001310013.1:n.385-146_385-145delinsTG