Canonical Allele Identifier: CA376035402

Gene: PHYH

Linked Data

• MyVariant Identifiers: chr10:g.13330432G>C (hg19) ; chr10:g.13288432G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13288432G>C , CM000672.2:g.13288432G>C	GRCh38
NC_000010.10:g.13330432G>C , CM000672.1:g.13330432G>C	GRCh37
NC_000010.9:g.13370438G>C	NCBI36
NG_012862.1:g.16699C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263038.9:c.606C>G MANE Select	ENSP00000263038.4:p.Asn202Lys
ENST00000263038.8:c.606C>G	ENSP00000263038.4:p.Asn202Lys
ENST00000396913.6:c.306C>G	ENSP00000380121.2:p.Asn102Lys
ENST00000396920.7:c.555C>G	ENSP00000380126.3:p.Asn185Lys
ENST00000453759.6:c.306C>G	ENSP00000412525.2:p.Asn102Lys
ENST00000479604.1:c.612C>G	ENSP00000420117.1:p.Asn204Lys
NM_001037537.1:c.306C>G	NP_001032626.1:p.Asn102Lys
NM_006214.3:c.606C>G	NP_006205.1:p.Asn202Lys
XM_005252469.2:c.460-4593C>G	XP_005252526.1:n.460-4593C>G
NM_001323080.1:c.306C>G	NP_001310009.1:p.Asn102Lys
NM_001323082.1:c.612C>G	NP_001310011.1:p.Asn204Lys
NM_001323083.1:c.415-4593C>G	NP_001310012.1:n.415-4593C>G
NM_001323084.1:c.312C>G	NP_001310013.1:p.Asn104Lys
NM_006214.4:c.606C>G MANE Select	NP_006205.1:p.Asn202Lys
NM_001037537.2:c.306C>G	NP_001032626.1:p.Asn102Lys
NM_001323080.2:c.306C>G	NP_001310009.1:p.Asn102Lys
NM_001323082.2:c.612C>G	NP_001310011.1:p.Asn204Lys
NM_001323083.2:c.415-4593C>G	NP_001310012.1:n.415-4593C>G
NM_001323084.2:c.312C>G	NP_001310013.1:p.Asn104Lys