Canonical Allele Identifier: CA2059430927
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102839219C= , CM000674.2:g.102839219C= GRCh38
NC_000012.11:g.103232997C= , CM000674.1:g.103232997C= GRCh37
NC_000012.10:g.101757127C= NCBI36
NG_008690.1:g.83384G=
NG_008690.2:g.124192G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1316-1G= MANE Select ENSP00000448059.1:n.1316-1G=
ENST00000307000.7:c.1301-1G= ENSP00000303500.2:n.1301-1G=
ENST00000551114.2:n.978-1G=
ENST00000553106.5:c.1316-1G= ENSP00000448059.1:n.1316-1G=
ENST00000635477.1:c.420-1G=
ENST00000635528.1:n.831-1G=
NM_000277.1:c.1316-1G= NP_000268.1:n.1316-1G=
XM_011538422.1:c.1259-1G= XP_011536724.1:n.1259-1G=
NM_000277.2:c.1316-1G= NP_000268.1:n.1316-1G=
NM_001354304.1:c.1316-1G= NP_001341233.1:n.1316-1G=
NM_000277.3:c.1316-1G= MANE Select NP_000268.1:n.1316-1G=
NM_001354304.2:c.1316-1G= NP_001341233.1:n.1316-1G=
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