Canonical Allele Identifier: CA2059444375
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102851697T= , CM000674.2:g.102851697T= GRCh38
NC_000012.11:g.103245475T= , CM000674.1:g.103245475T= GRCh37
NC_000012.10:g.101769605T= NCBI36
NG_008690.1:g.70906A=
NG_008690.2:g.111714A=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.902A= MANE Select ENSP00000448059.1:p.Gln301=
ENST00000307000.7:c.887A= ENSP00000303500.2:p.Gln296=
ENST00000549247.6:n.661A=
ENST00000551114.2:n.564A=
ENST00000553106.5:c.902A= ENSP00000448059.1:p.Gln301=
ENST00000635477.1:c.63A=
NM_000277.1:c.902A= NP_000268.1:p.Gln301=
XM_011538422.1:c.902A= XP_011536724.1:p.Gln301=
NM_000277.2:c.902A= NP_000268.1:p.Gln301=
NM_001354304.1:c.902A= NP_001341233.1:p.Gln301=
NM_000277.3:c.902A= MANE Select NP_000268.1:p.Gln301=
NM_001354304.2:c.902A= NP_001341233.1:p.Gln301=
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