Canonical Allele Identifier: CA2059451225
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846883G= , CM000674.2:g.102846883G= GRCh38
NC_000012.11:g.103240661G= , CM000674.1:g.103240661G= GRCh37
NC_000012.10:g.101764791G= NCBI36
NG_008690.1:g.75720C=
NG_008690.2:g.116528C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.969+12C= MANE Select ENSP00000448059.1:n.969+12C=
ENST00000307000.7:c.954+12C= ENSP00000303500.2:n.954+12C=
ENST00000549247.6:n.728+12C=
ENST00000551114.2:n.631+12C=
ENST00000553106.5:c.969+12C= ENSP00000448059.1:n.969+12C=
ENST00000635477.1:c.74-2452C=
ENST00000635528.1:n.484+12C=
NM_000277.1:c.969+12C= NP_000268.1:n.969+12C=
XM_011538422.1:c.913-2452C= XP_011536724.1:n.913-2452C=
NM_000277.2:c.969+12C= NP_000268.1:n.969+12C=
NM_001354304.1:c.969+12C= NP_001341233.1:n.969+12C=
NM_000277.3:c.969+12C= MANE Select NP_000268.1:n.969+12C=
NM_001354304.2:c.969+12C= NP_001341233.1:n.969+12C=
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