Canonical Allele Identifier: CA2059444063

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102851473G= , CM000674.2:g.102851473G=	GRCh38
NC_000012.11:g.103245251G= , CM000674.1:g.103245251G=	GRCh37
NC_000012.10:g.101769381G=	NCBI36
NG_008690.1:g.71130C=
NG_008690.2:g.111938C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.912+214C= MANE Select	ENSP00000448059.1:n.912+214C=
ENST00000307000.7:c.897+214C=	ENSP00000303500.2:n.897+214C=
ENST00000549247.6:n.671+214C=
ENST00000551114.2:n.574+214C=
ENST00000553106.5:c.912+214C=	ENSP00000448059.1:n.912+214C=
ENST00000635477.1:c.73+214C=
NM_000277.1:c.912+214C=	NP_000268.1:n.912+214C=
XM_011538422.1:c.912+214C=	XP_011536724.1:n.912+214C=
NM_000277.2:c.912+214C=	NP_000268.1:n.912+214C=
NM_001354304.1:c.912+214C=	NP_001341233.1:n.912+214C=
NM_000277.3:c.912+214C= MANE Select	NP_000268.1:n.912+214C=
NM_001354304.2:c.912+214C=	NP_001341233.1:n.912+214C=