Canonical Allele Identifier: CA2059443671

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102851163G= , CM000674.2:g.102851163G=	GRCh38
NC_000012.11:g.103244941G= , CM000674.1:g.103244941G=	GRCh37
NC_000012.10:g.101769071G=	NCBI36
NG_008690.1:g.71440C=
NG_008690.2:g.112248C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.912+524C= MANE Select	ENSP00000448059.1:n.912+524C=
ENST00000307000.7:c.897+524C=	ENSP00000303500.2:n.897+524C=
ENST00000549247.6:n.671+524C=
ENST00000551114.2:n.574+524C=
ENST00000553106.5:c.912+524C=	ENSP00000448059.1:n.912+524C=
ENST00000635477.1:c.73+524C=
NM_000277.1:c.912+524C=	NP_000268.1:n.912+524C=
XM_011538422.1:c.912+524C=	XP_011536724.1:n.912+524C=
NM_000277.2:c.912+524C=	NP_000268.1:n.912+524C=
NM_001354304.1:c.912+524C=	NP_001341233.1:n.912+524C=
NM_000277.3:c.912+524C= MANE Select	NP_000268.1:n.912+524C=
NM_001354304.2:c.912+524C=	NP_001341233.1:n.912+524C=