Canonical Allele Identifier: CA468236832

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325714C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283714C>T , CM000672.2:g.13283714C>T	GRCh38
NC_000010.10:g.13325714C>T , CM000672.1:g.13325714C>T	GRCh37
NC_000010.9:g.13365720C>T	NCBI36
NG_012862.1:g.21417G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.804G>A MANE Select	ENSP00000263038.4:p.Gln268=
ENST00000263038.8:c.804G>A	ENSP00000263038.4:p.Gln268=
ENST00000396913.6:c.504G>A	ENSP00000380121.2:p.Gln168=
ENST00000396920.7:c.753G>A	ENSP00000380126.3:p.Gln251=
ENST00000453759.6:c.504G>A	ENSP00000412525.2:p.Gln168=
NM_001037537.1:c.504G>A	NP_001032626.1:p.Gln168=
NM_006214.3:c.804G>A	NP_006205.1:p.Gln268=
XM_005252469.2:c.585G>A	XP_005252526.1:p.Gln195=
NM_001323080.1:c.504G>A	NP_001310009.1:p.Gln168=
NM_001323082.1:c.810G>A	NP_001310011.1:p.Gln270=
NM_001323083.1:c.540G>A	NP_001310012.1:p.Gln180=
NM_001323084.1:c.510G>A	NP_001310013.1:p.Gln170=
NM_006214.4:c.804G>A MANE Select	NP_006205.1:p.Gln268=
NM_001037537.2:c.504G>A	NP_001032626.1:p.Gln168=
NM_001323080.2:c.504G>A	NP_001310009.1:p.Gln168=
NM_001323082.2:c.810G>A	NP_001310011.1:p.Gln270=
NM_001323083.2:c.540G>A	NP_001310012.1:p.Gln180=
NM_001323084.2:c.510G>A	NP_001310013.1:p.Gln170=