Canonical Allele Identifier: CA2059473512

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102912888T= , CM000674.2:g.102912888T=	GRCh38
NC_000012.11:g.103306666T= , CM000674.1:g.103306666T=	GRCh37
NC_000012.10:g.101830796T=	NCBI36
NG_008690.1:g.9715A=
NG_008690.2:g.50523A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.71A= MANE Select	ENSP00000448059.1:p.Tyr24=
ENST00000307000.7:c.56A=	ENSP00000303500.2:p.Tyr19=
ENST00000546844.1:c.71A=	ENSP00000446658.1:p.Tyr24=
ENST00000548677.2:n.158A=
ENST00000549111.5:n.167A=
ENST00000550978.6:c.55A=
ENST00000551337.5:c.71A=	ENSP00000447620.1:p.Tyr24=
ENST00000551988.5:n.160A=
ENST00000553106.5:c.71A=	ENSP00000448059.1:p.Tyr24=
ENST00000635500.1:n.39A=
NM_000277.1:c.71A=	NP_000268.1:p.Tyr24=
XM_011538422.1:c.71A=	XP_011536724.1:p.Tyr24=
NM_000277.2:c.71A=	NP_000268.1:p.Tyr24=
NM_001354304.1:c.71A=	NP_001341233.1:p.Tyr24=
XM_017019370.2:c.71A=	XP_016874859.1:p.Tyr24=
NM_000277.3:c.71A= MANE Select	NP_000268.1:p.Tyr24=
NM_001354304.2:c.71A=	NP_001341233.1:p.Tyr24=