Canonical Allele Identifier: CA2059476166

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102917097C= , CM000674.2:g.102917097C=	GRCh38
NC_000012.11:g.103310875C= , CM000674.1:g.103310875C=	GRCh37
NC_000012.10:g.101835005C=	NCBI36
NG_008690.1:g.5506G=
NG_008690.2:g.46314G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.34G= MANE Select	ENSP00000448059.1:p.Gly12=
ENST00000307000.7:c.-114G=	ENSP00000303500.2:n.-114G=
ENST00000546844.1:c.34G=	ENSP00000446658.1:p.Gly12=
ENST00000547319.1:n.345G=
ENST00000549111.5:n.130G=
ENST00000550978.6:c.18G=
ENST00000551337.5:c.34G=	ENSP00000447620.1:p.Gly12=
ENST00000551988.5:n.123G=
ENST00000553106.5:c.34G=	ENSP00000448059.1:p.Gly12=
ENST00000635500.1:n.29-4199G=
NM_000277.1:c.34G=	NP_000268.1:p.Gly12=
XM_011538422.1:c.34G=	XP_011536724.1:p.Gly12=
NM_000277.2:c.34G=	NP_000268.1:p.Gly12=
NM_001354304.1:c.34G=	NP_001341233.1:p.Gly12=
XM_017019370.2:c.34G=	XP_016874859.1:p.Gly12=
NM_000277.3:c.34G= MANE Select	NP_000268.1:p.Gly12=
NM_001354304.2:c.34G=	NP_001341233.1:p.Gly12=