Canonical Allele Identifier: CA468237053

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325780C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283780C>T , CM000672.2:g.13283780C>T	GRCh38
NC_000010.10:g.13325780C>T , CM000672.1:g.13325780C>T	GRCh37
NC_000010.9:g.13365786C>T	NCBI36
NG_012862.1:g.21351G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.738G>A MANE Select	ENSP00000263038.4:p.Val246=
ENST00000263038.8:c.738G>A	ENSP00000263038.4:p.Val246=
ENST00000396913.6:c.438G>A	ENSP00000380121.2:p.Val146=
ENST00000396920.7:c.687G>A	ENSP00000380126.3:p.Val229=
ENST00000453759.6:c.438G>A	ENSP00000412525.2:p.Val146=
NM_001037537.1:c.438G>A	NP_001032626.1:p.Val146=
NM_006214.3:c.738G>A	NP_006205.1:p.Val246=
XM_005252469.2:c.519G>A	XP_005252526.1:p.Val173=
NM_001323080.1:c.438G>A	NP_001310009.1:p.Val146=
NM_001323082.1:c.744G>A	NP_001310011.1:p.Val248=
NM_001323083.1:c.474G>A	NP_001310012.1:p.Val158=
NM_001323084.1:c.444G>A	NP_001310013.1:p.Val148=
NM_006214.4:c.738G>A MANE Select	NP_006205.1:p.Val246=
NM_001037537.2:c.438G>A	NP_001032626.1:p.Val146=
NM_001323080.2:c.438G>A	NP_001310009.1:p.Val146=
NM_001323082.2:c.744G>A	NP_001310011.1:p.Val248=
NM_001323083.2:c.474G>A	NP_001310012.1:p.Val158=
NM_001323084.2:c.444G>A	NP_001310013.1:p.Val148=