Canonical Allele Identifier: CA2059447027

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102843808C= , CM000674.2:g.102843808C=	GRCh38
NC_000012.11:g.103237586C= , CM000674.1:g.103237586C=	GRCh37
NC_000012.10:g.101761716C=	NCBI36
NG_008690.1:g.78795G=
NG_008690.2:g.119603G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.1066-29G= MANE Select	ENSP00000448059.1:n.1066-29G=
ENST00000307000.7:c.1051-29G=	ENSP00000303500.2:n.1051-29G=
ENST00000549247.6:n.825-29G=
ENST00000551114.2:n.728-29G=
ENST00000553106.5:c.1066-29G=	ENSP00000448059.1:n.1066-29G=
ENST00000635477.1:c.170-29G=
ENST00000635528.1:n.581-29G=
NM_000277.1:c.1066-29G=	NP_000268.1:n.1066-29G=
XM_011538422.1:c.1009-29G=	XP_011536724.1:n.1009-29G=
NM_000277.2:c.1066-29G=	NP_000268.1:n.1066-29G=
NM_001354304.1:c.1066-29G=	NP_001341233.1:n.1066-29G=
NM_000277.3:c.1066-29G= MANE Select	NP_000268.1:n.1066-29G=
NM_001354304.2:c.1066-29G=	NP_001341233.1:n.1066-29G=