Canonical Allele Identifier: CA1891546633

Gene: PHYH

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283813C= , CM000672.2:g.13283813C=	GRCh38
NC_000010.10:g.13325813C= , CM000672.1:g.13325813C=	GRCh37
NC_000010.9:g.13365819C=	NCBI36
NG_012862.1:g.21318G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263038.9:c.705G= MANE Select	ENSP00000263038.4:p.Gly235=
ENST00000263038.8:c.705G=	ENSP00000263038.4:p.Gly235=
ENST00000396913.6:c.405G=	ENSP00000380121.2:p.Gly135=
ENST00000396920.7:c.654G=	ENSP00000380126.3:p.Gly218=
ENST00000453759.6:c.405G=	ENSP00000412525.2:p.Gly135=
NM_001037537.1:c.405G=	NP_001032626.1:p.Gly135=
NM_006214.3:c.705G=	NP_006205.1:p.Gly235=
XM_005252469.2:c.486G=	XP_005252526.1:p.Gly162=
NM_001323080.1:c.405G=	NP_001310009.1:p.Gly135=
NM_001323082.1:c.711G=	NP_001310011.1:p.Gly237=
NM_001323083.1:c.441G=	NP_001310012.1:p.Gly147=
NM_001323084.1:c.411G=	NP_001310013.1:p.Gly137=
NM_006214.4:c.705G= MANE Select	NP_006205.1:p.Gly235=
NM_001037537.2:c.405G=	NP_001032626.1:p.Gly135=
NM_001323080.2:c.405G=	NP_001310009.1:p.Gly135=
NM_001323082.2:c.711G=	NP_001310011.1:p.Gly237=
NM_001323083.2:c.441G=	NP_001310012.1:p.Gly147=
NM_001323084.2:c.411G=	NP_001310013.1:p.Gly137=