Canonical Allele Identifier: CA2059466525
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894724C= , CM000674.2:g.102894724C= GRCh38
NC_000012.11:g.103288502C= , CM000674.1:g.103288502C= GRCh37
NC_000012.10:g.101812632C= NCBI36
NG_008690.1:g.27879G=
NG_008690.2:g.68687G=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.352+11G= MANE Select ENSP00000448059.1:n.352+11G=
ENST00000307000.7:c.337+11G= ENSP00000303500.2:n.337+11G=
ENST00000548928.1:n.274+11G=
ENST00000549111.5:n.448+11G=
ENST00000550978.6:c.336+11G=
ENST00000551337.5:c.352+11G= ENSP00000447620.1:n.352+11G=
ENST00000551988.5:n.441+11G=
ENST00000553106.5:c.352+11G= ENSP00000448059.1:n.352+11G=
NM_000277.1:c.352+11G= NP_000268.1:n.352+11G=
XM_011538422.1:c.352+11G= XP_011536724.1:n.352+11G=
NM_000277.2:c.352+11G= NP_000268.1:n.352+11G=
NM_001354304.1:c.352+11G= NP_001341233.1:n.352+11G=
XM_017019370.2:c.352+11G= XP_016874859.1:n.352+11G=
NM_000277.3:c.352+11G= MANE Select NP_000268.1:n.352+11G=
NM_001354304.2:c.352+11G= NP_001341233.1:n.352+11G=
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