Canonical Allele Identifier: CA2059444435

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102851703A= , CM000674.2:g.102851703A=	GRCh38
NC_000012.11:g.103245481A= , CM000674.1:g.103245481A=	GRCh37
NC_000012.10:g.101769611A=	NCBI36
NG_008690.1:g.70900T=
NG_008690.2:g.111708T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.896T= MANE Select	ENSP00000448059.1:p.Phe299=
ENST00000307000.7:c.881T=	ENSP00000303500.2:p.Phe294=
ENST00000549247.6:n.655T=
ENST00000551114.2:n.558T=
ENST00000553106.5:c.896T=	ENSP00000448059.1:p.Phe299=
ENST00000635477.1:c.57T=
NM_000277.1:c.896T=	NP_000268.1:p.Phe299=
XM_011538422.1:c.896T=	XP_011536724.1:p.Phe299=
NM_000277.2:c.896T=	NP_000268.1:p.Phe299=
NM_001354304.1:c.896T=	NP_001341233.1:p.Phe299=
NM_000277.3:c.896T= MANE Select	NP_000268.1:p.Phe299=
NM_001354304.2:c.896T=	NP_001341233.1:p.Phe299=