Canonical Allele Identifier: CA2059446912
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843778T= , CM000674.2:g.102843778T= GRCh38
NC_000012.11:g.103237556T= , CM000674.1:g.103237556T= GRCh37
NC_000012.10:g.101761686T= NCBI36
NG_008690.1:g.78825A=
NG_008690.2:g.119633A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1067A= MANE Select ENSP00000448059.1:p.Tyr356=
ENST00000307000.7:c.1052A= ENSP00000303500.2:p.Tyr351=
ENST00000549247.6:n.826A=
ENST00000551114.2:n.729A=
ENST00000553106.5:c.1067A= ENSP00000448059.1:p.Tyr356=
ENST00000635477.1:c.171A=
ENST00000635528.1:n.582A=
NM_000277.1:c.1067A= NP_000268.1:p.Tyr356=
XM_011538422.1:c.1010A= XP_011536724.1:p.Tyr337=
NM_000277.2:c.1067A= NP_000268.1:p.Tyr356=
NM_001354304.1:c.1067A= NP_001341233.1:p.Tyr356=
NM_000277.3:c.1067A= MANE Select NP_000268.1:p.Tyr356=
NM_001354304.2:c.1067A= NP_001341233.1:p.Tyr356=
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