Canonical Allele Identifier: CA2059476274
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917298G= , CM000674.2:g.102917298G= GRCh38
NC_000012.11:g.103311076G= , CM000674.1:g.103311076G= GRCh37
NC_000012.10:g.101835206G= NCBI36
NG_008690.1:g.5305C=
NG_008690.2:g.46113C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-73C=
ENST00000546844.1:c.-95-73C= ENSP00000446658.1:n.-95-73C=
ENST00000547319.1:n.217-73C=
ENST00000551337.5:c.-95-73C= ENSP00000447620.1:n.-95-73C=
ENST00000553106.5:c.-168C= ENSP00000448059.1:n.-168C=
ENST00000635500.1:n.29-4400C=
NM_000277.1:c.-168C= NP_000268.1:n.-168C=
NM_000277.2:c.-168C= NP_000268.1:n.-168C=
NM_001354304.1:c.-95-73C= NP_001341233.1:n.-95-73C=
NM_001354304.2:c.-95-73C= NP_001341233.1:n.-95-73C=