Canonical Allele Identifier: CA2059448111
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844358A= , CM000674.2:g.102844358A= GRCh38
NC_000012.11:g.103238136A= , CM000674.1:g.103238136A= GRCh37
NC_000012.10:g.101762266A= NCBI36
NG_008690.1:g.78245T=
NG_008690.2:g.119053T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1043T= MANE Select ENSP00000448059.1:p.Leu348=
ENST00000307000.7:c.1028T= ENSP00000303500.2:p.Leu343=
ENST00000549247.6:n.802T=
ENST00000551114.2:n.705T=
ENST00000553106.5:c.1043T= ENSP00000448059.1:p.Leu348=
ENST00000635477.1:c.147T=
ENST00000635528.1:n.558T=
NM_000277.1:c.1043T= NP_000268.1:p.Leu348=
XM_011538422.1:c.986T= XP_011536724.1:p.Leu329=
NM_000277.2:c.1043T= NP_000268.1:p.Leu348=
NM_001354304.1:c.1043T= NP_001341233.1:p.Leu348=
NM_000277.3:c.1043T= MANE Select NP_000268.1:p.Leu348=
NM_001354304.2:c.1043T= NP_001341233.1:p.Leu348=
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