Canonical Allele Identifier: CA2059476238
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917253G= , CM000674.2:g.102917253G= GRCh38
NC_000012.11:g.103311031G= , CM000674.1:g.103311031G= GRCh37
NC_000012.10:g.101835161G= NCBI36
NG_008690.1:g.5350C=
NG_008690.2:g.46158C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307000.7:c.-270C= ENSP00000303500.2:n.-270C=
ENST00000546708.5:n.493-28C=
ENST00000546844.1:c.-95-28C= ENSP00000446658.1:n.-95-28C=
ENST00000547319.1:n.217-28C=
ENST00000551337.5:c.-95-28C= ENSP00000447620.1:n.-95-28C=
ENST00000553106.5:c.-123C= ENSP00000448059.1:n.-123C=
ENST00000635500.1:n.29-4355C=
NM_000277.1:c.-123C= NP_000268.1:n.-123C=
NM_000277.2:c.-123C= NP_000268.1:n.-123C=
NM_001354304.1:c.-95-28C= NP_001341233.1:n.-95-28C=
NM_001354304.2:c.-95-28C= NP_001341233.1:n.-95-28C=