Canonical Allele Identifier: CA376034211

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325767C>G (hg19) ; chr10:g.13283767C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283767C>G , CM000672.2:g.13283767C>G	GRCh38
NC_000010.10:g.13325767C>G , CM000672.1:g.13325767C>G	GRCh37
NC_000010.9:g.13365773C>G	NCBI36
NG_012862.1:g.21364G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.751G>C MANE Select	ENSP00000263038.4:p.Glu251Gln
ENST00000263038.8:c.751G>C	ENSP00000263038.4:p.Glu251Gln
ENST00000396913.6:c.451G>C	ENSP00000380121.2:p.Glu151Gln
ENST00000396920.7:c.700G>C	ENSP00000380126.3:p.Glu234Gln
ENST00000453759.6:c.451G>C	ENSP00000412525.2:p.Glu151Gln
NM_001037537.1:c.451G>C	NP_001032626.1:p.Glu151Gln
NM_006214.3:c.751G>C	NP_006205.1:p.Glu251Gln
XM_005252469.2:c.532G>C	XP_005252526.1:p.Glu178Gln
NM_001323080.1:c.451G>C	NP_001310009.1:p.Glu151Gln
NM_001323082.1:c.757G>C	NP_001310011.1:p.Glu253Gln
NM_001323083.1:c.487G>C	NP_001310012.1:p.Glu163Gln
NM_001323084.1:c.457G>C	NP_001310013.1:p.Glu153Gln
NM_006214.4:c.751G>C MANE Select	NP_006205.1:p.Glu251Gln
NM_001037537.2:c.451G>C	NP_001032626.1:p.Glu151Gln
NM_001323080.2:c.451G>C	NP_001310009.1:p.Glu151Gln
NM_001323082.2:c.757G>C	NP_001310011.1:p.Glu253Gln
NM_001323083.2:c.487G>C	NP_001310012.1:p.Glu163Gln
NM_001323084.2:c.457G>C	NP_001310013.1:p.Glu153Gln