Canonical Allele Identifier: CA2059451172

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102846849T= , CM000674.2:g.102846849T=	GRCh38
NC_000012.11:g.103240627T= , CM000674.1:g.103240627T=	GRCh37
NC_000012.10:g.101764757T=	NCBI36
NG_008690.1:g.75754A=
NG_008690.2:g.116562A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.969+46A= MANE Select	ENSP00000448059.1:n.969+46A=
ENST00000307000.7:c.954+46A=	ENSP00000303500.2:n.954+46A=
ENST00000549247.6:n.728+46A=
ENST00000551114.2:n.631+46A=
ENST00000553106.5:c.969+46A=	ENSP00000448059.1:n.969+46A=
ENST00000635477.1:c.74-2418A=
ENST00000635528.1:n.484+46A=
NM_000277.1:c.969+46A=	NP_000268.1:n.969+46A=
XM_011538422.1:c.913-2418A=	XP_011536724.1:n.913-2418A=
NM_000277.2:c.969+46A=	NP_000268.1:n.969+46A=
NM_001354304.1:c.969+46A=	NP_001341233.1:n.969+46A=
NM_000277.3:c.969+46A= MANE Select	NP_000268.1:n.969+46A=
NM_001354304.2:c.969+46A=	NP_001341233.1:n.969+46A=