Canonical Allele Identifier: CA376034296

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325788C>A (hg19) ; chr10:g.13283788C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283788C>A , CM000672.2:g.13283788C>A	GRCh38
NC_000010.10:g.13325788C>A , CM000672.1:g.13325788C>A	GRCh37
NC_000010.9:g.13365794C>A	NCBI36
NG_012862.1:g.21343G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.730G>T MANE Select	ENSP00000263038.4:p.Ala244Ser
ENST00000263038.8:c.730G>T	ENSP00000263038.4:p.Ala244Ser
ENST00000396913.6:c.430G>T	ENSP00000380121.2:p.Ala144Ser
ENST00000396920.7:c.679G>T	ENSP00000380126.3:p.Ala227Ser
ENST00000453759.6:c.430G>T	ENSP00000412525.2:p.Ala144Ser
NM_001037537.1:c.430G>T	NP_001032626.1:p.Ala144Ser
NM_006214.3:c.730G>T	NP_006205.1:p.Ala244Ser
XM_005252469.2:c.511G>T	XP_005252526.1:p.Ala171Ser
NM_001323080.1:c.430G>T	NP_001310009.1:p.Ala144Ser
NM_001323082.1:c.736G>T	NP_001310011.1:p.Ala246Ser
NM_001323083.1:c.466G>T	NP_001310012.1:p.Ala156Ser
NM_001323084.1:c.436G>T	NP_001310013.1:p.Ala146Ser
NM_006214.4:c.730G>T MANE Select	NP_006205.1:p.Ala244Ser
NM_001037537.2:c.430G>T	NP_001032626.1:p.Ala144Ser
NM_001323080.2:c.430G>T	NP_001310009.1:p.Ala144Ser
NM_001323082.2:c.736G>T	NP_001310011.1:p.Ala246Ser
NM_001323083.2:c.466G>T	NP_001310012.1:p.Ala156Ser
NM_001323084.2:c.436G>T	NP_001310013.1:p.Ala146Ser