Canonical Allele Identifier: CA2059449037
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855143G= , CM000674.2:g.102855143G= GRCh38
NC_000012.11:g.103248921G= , CM000674.1:g.103248921G= GRCh37
NC_000012.10:g.101773051G= NCBI36
NG_008690.1:g.67460C=
NG_008690.2:g.108268C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.699C= MANE Select ENSP00000448059.1:p.Phe233=
ENST00000307000.7:c.684C= ENSP00000303500.2:p.Phe228=
ENST00000549111.5:n.795C=
ENST00000553106.5:c.699C= ENSP00000448059.1:p.Phe233=
NM_000277.1:c.699C= NP_000268.1:p.Phe233=
XM_011538422.1:c.699C= XP_011536724.1:p.Phe233=
NM_000277.2:c.699C= NP_000268.1:p.Phe233=
NM_001354304.1:c.699C= NP_001341233.1:p.Phe233=
XM_017019370.2:c.699C= XP_016874859.1:p.Phe233=
NM_000277.3:c.699C= MANE Select NP_000268.1:p.Phe233=
NM_001354304.2:c.699C= NP_001341233.1:p.Phe233=