Canonical Allele Identifier: CA2059451339
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846917T= , CM000674.2:g.102846917T= GRCh38
NC_000012.11:g.103240695T= , CM000674.1:g.103240695T= GRCh37
NC_000012.10:g.101764825T= NCBI36
NG_008690.1:g.75686A=
NG_008690.2:g.116494A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.947A= MANE Select ENSP00000448059.1:p.Glu316=
ENST00000307000.7:c.932A= ENSP00000303500.2:p.Glu311=
ENST00000549247.6:n.706A=
ENST00000551114.2:n.609A=
ENST00000553106.5:c.947A= ENSP00000448059.1:p.Glu316=
ENST00000635477.1:c.74-2486A=
ENST00000635528.1:n.462A=
NM_000277.1:c.947A= NP_000268.1:p.Glu316=
XM_011538422.1:c.913-2486A= XP_011536724.1:n.913-2486A=
NM_000277.2:c.947A= NP_000268.1:p.Glu316=
NM_001354304.1:c.947A= NP_001341233.1:p.Glu316=
NM_000277.3:c.947A= MANE Select NP_000268.1:p.Glu316=
NM_001354304.2:c.947A= NP_001341233.1:p.Glu316=