Canonical Allele Identifier: CA2059456928
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866518C= , CM000674.2:g.102866518C= GRCh38
NC_000012.11:g.103260296C= , CM000674.1:g.103260296C= GRCh37
NC_000012.10:g.101784426C= NCBI36
NG_008690.1:g.56085G=
NG_008690.2:g.96893G=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.509+78G= MANE Select ENSP00000448059.1:n.509+78G=
ENST00000307000.7:c.494+78G= ENSP00000303500.2:n.494+78G=
ENST00000549111.5:n.605+78G=
ENST00000551988.5:n.530+10944G=
ENST00000553106.5:c.509+78G= ENSP00000448059.1:n.509+78G=
NM_000277.1:c.509+78G= NP_000268.1:n.509+78G=
XM_011538422.1:c.509+78G= XP_011536724.1:n.509+78G=
NM_000277.2:c.509+78G= NP_000268.1:n.509+78G=
NM_001354304.1:c.509+78G= NP_001341233.1:n.509+78G=
XM_017019370.2:c.509+78G= XP_016874859.1:n.509+78G=
NM_000277.3:c.509+78G= MANE Select NP_000268.1:n.509+78G=
NM_001354304.2:c.509+78G= NP_001341233.1:n.509+78G=
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