Canonical Allele Identifier: CA468236763

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13325693C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13283693C>T , CM000672.2:g.13283693C>T	GRCh38
NC_000010.10:g.13325693C>T , CM000672.1:g.13325693C>T	GRCh37
NC_000010.9:g.13365699C>T	NCBI36
NG_012862.1:g.21438G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.825G>A MANE Select	ENSP00000263038.4:p.Arg275=
ENST00000263038.8:c.825G>A	ENSP00000263038.4:p.Arg275=
ENST00000396913.6:c.525G>A	ENSP00000380121.2:p.Arg175=
ENST00000396920.7:c.774G>A	ENSP00000380126.3:p.Arg258=
ENST00000453759.6:c.525G>A	ENSP00000412525.2:p.Arg175=
NM_001037537.1:c.525G>A	NP_001032626.1:p.Arg175=
NM_006214.3:c.825G>A	NP_006205.1:p.Arg275=
XM_005252469.2:c.606G>A	XP_005252526.1:p.Arg202=
NM_001323080.1:c.525G>A	NP_001310009.1:p.Arg175=
NM_001323082.1:c.831G>A	NP_001310011.1:p.Arg277=
NM_001323083.1:c.561G>A	NP_001310012.1:p.Arg187=
NM_001323084.1:c.531G>A	NP_001310013.1:p.Arg177=
NM_006214.4:c.825G>A MANE Select	NP_006205.1:p.Arg275=
NM_001037537.2:c.525G>A	NP_001032626.1:p.Arg175=
NM_001323080.2:c.525G>A	NP_001310009.1:p.Arg175=
NM_001323082.2:c.831G>A	NP_001310011.1:p.Arg277=
NM_001323083.2:c.561G>A	NP_001310012.1:p.Arg187=
NM_001323084.2:c.531G>A	NP_001310013.1:p.Arg177=