Canonical Allele Identifier: CA2059476195
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917147T= , CM000674.2:g.102917147T= GRCh38
NC_000012.11:g.103310925T= , CM000674.1:g.103310925T= GRCh37
NC_000012.10:g.101835055T= NCBI36
NG_008690.1:g.5456A=
NG_008690.2:g.46264A=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.-17A= MANE Select ENSP00000448059.1:n.-17A=
ENST00000307000.7:c.-164A= ENSP00000303500.2:n.-164A=
ENST00000546844.1:c.-17A= ENSP00000446658.1:n.-17A=
ENST00000547319.1:n.295A=
ENST00000549111.5:n.80A=
ENST00000551337.5:c.-17A= ENSP00000447620.1:n.-17A=
ENST00000551988.5:n.73A=
ENST00000553106.5:c.-17A= ENSP00000448059.1:n.-17A=
ENST00000635500.1:n.29-4249A=
NM_000277.1:c.-17A= NP_000268.1:n.-17A=
XM_011538422.1:c.-17A= XP_011536724.1:n.-17A=
NM_000277.2:c.-17A= NP_000268.1:n.-17A=
NM_001354304.1:c.-17A= NP_001341233.1:n.-17A=
XM_017019370.2:c.-17A= XP_016874859.1:n.-17A=
NM_000277.3:c.-17A= MANE Select NP_000268.1:n.-17A=
NM_001354304.2:c.-17A= NP_001341233.1:n.-17A=
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