Canonical Allele Identifier: CA2059447018

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102843801T= , CM000674.2:g.102843801T=	GRCh38
NC_000012.11:g.103237579T= , CM000674.1:g.103237579T=	GRCh37
NC_000012.10:g.101761709T=	NCBI36
NG_008690.1:g.78802A=
NG_008690.2:g.119610A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.1066-22A= MANE Select	ENSP00000448059.1:n.1066-22A=
ENST00000307000.7:c.1051-22A=	ENSP00000303500.2:n.1051-22A=
ENST00000549247.6:n.825-22A=
ENST00000551114.2:n.728-22A=
ENST00000553106.5:c.1066-22A=	ENSP00000448059.1:n.1066-22A=
ENST00000635477.1:c.170-22A=
ENST00000635528.1:n.581-22A=
NM_000277.1:c.1066-22A=	NP_000268.1:n.1066-22A=
XM_011538422.1:c.1009-22A=	XP_011536724.1:n.1009-22A=
NM_000277.2:c.1066-22A=	NP_000268.1:n.1066-22A=
NM_001354304.1:c.1066-22A=	NP_001341233.1:n.1066-22A=
NM_000277.3:c.1066-22A= MANE Select	NP_000268.1:n.1066-22A=
NM_001354304.2:c.1066-22A=	NP_001341233.1:n.1066-22A=