Canonical Allele Identifier: CA2059473592

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102912990T= , CM000674.2:g.102912990T=	GRCh38
NC_000012.11:g.103306768T= , CM000674.1:g.103306768T=	GRCh37
NC_000012.10:g.101830898T=	NCBI36
NG_008690.1:g.9613A=
NG_008690.2:g.50421A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.61-92A= MANE Select	ENSP00000448059.1:n.61-92A=
ENST00000307000.7:c.46-92A=	ENSP00000303500.2:n.46-92A=
ENST00000546844.1:c.61-92A=	ENSP00000446658.1:n.61-92A=
ENST00000548677.2:n.148-92A=
ENST00000549111.5:n.157-92A=
ENST00000550978.6:c.45-92A=
ENST00000551337.5:c.61-92A=	ENSP00000447620.1:n.61-92A=
ENST00000551988.5:n.150-92A=
ENST00000553106.5:c.61-92A=	ENSP00000448059.1:n.61-92A=
ENST00000635500.1:n.29-92A=
NM_000277.1:c.61-92A=	NP_000268.1:n.61-92A=
XM_011538422.1:c.61-92A=	XP_011536724.1:n.61-92A=
NM_000277.2:c.61-92A=	NP_000268.1:n.61-92A=
NM_001354304.1:c.61-92A=	NP_001341233.1:n.61-92A=
XM_017019370.2:c.61-92A=	XP_016874859.1:n.61-92A=
NM_000277.3:c.61-92A= MANE Select	NP_000268.1:n.61-92A=
NM_001354304.2:c.61-92A=	NP_001341233.1:n.61-92A=