Canonical Allele Identifier: CA2059467011

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102894879A= , CM000674.2:g.102894879A=	GRCh38
NC_000012.11:g.103288657A= , CM000674.1:g.103288657A=	GRCh37
NC_000012.10:g.101812787A=	NCBI36
NG_008690.1:g.27724T=
NG_008690.2:g.68532T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.208T= MANE Select	ENSP00000448059.1:p.Ser70=
ENST00000307000.7:c.193T=	ENSP00000303500.2:p.Ser65=
ENST00000546844.1:c.208T=	ENSP00000446658.1:p.Ser70=
ENST00000548677.2:n.295T=
ENST00000548928.1:n.130T=
ENST00000549111.5:n.304T=
ENST00000550978.6:c.192T=
ENST00000551337.5:c.208T=	ENSP00000447620.1:p.Ser70=
ENST00000551988.5:n.297T=
ENST00000553106.5:c.208T=	ENSP00000448059.1:p.Ser70=
ENST00000635500.1:n.176T=
NM_000277.1:c.208T=	NP_000268.1:p.Ser70=
XM_011538422.1:c.208T=	XP_011536724.1:p.Ser70=
NM_000277.2:c.208T=	NP_000268.1:p.Ser70=
NM_001354304.1:c.208T=	NP_001341233.1:p.Ser70=
XM_017019370.2:c.208T=	XP_016874859.1:p.Ser70=
NM_000277.3:c.208T= MANE Select	NP_000268.1:p.Ser70=
NM_001354304.2:c.208T=	NP_001341233.1:p.Ser70=