Canonical Allele Identifier: CA2059462383

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102877347A= , CM000674.2:g.102877347A=	GRCh38
NC_000012.11:g.103271125A= , CM000674.1:g.103271125A=	GRCh37
NC_000012.10:g.101795255A=	NCBI36
NG_008690.1:g.45256T=
NG_008690.2:g.86064T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.441+115T= MANE Select	ENSP00000448059.1:n.441+115T=
ENST00000307000.7:c.426+115T=	ENSP00000303500.2:n.426+115T=
ENST00000549111.5:n.537+115T=
ENST00000550978.6:c.540T=
ENST00000551988.5:n.530+115T=
ENST00000553106.5:c.441+115T=	ENSP00000448059.1:n.441+115T=
NM_000277.1:c.441+115T=	NP_000268.1:n.441+115T=
XM_011538422.1:c.441+115T=	XP_011536724.1:n.441+115T=
NM_000277.2:c.441+115T=	NP_000268.1:n.441+115T=
NM_001354304.1:c.441+115T=	NP_001341233.1:n.441+115T=
XM_017019370.2:c.441+115T=	XP_016874859.1:n.441+115T=
NM_000277.3:c.441+115T= MANE Select	NP_000268.1:n.441+115T=
NM_001354304.2:c.441+115T=	NP_001341233.1:n.441+115T=