Canonical Allele Identifier: CA2059476273
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917295T= , CM000674.2:g.102917295T= GRCh38
NC_000012.11:g.103311073T= , CM000674.1:g.103311073T= GRCh37
NC_000012.10:g.101835203T= NCBI36
NG_008690.1:g.5308A=
NG_008690.2:g.46116A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-70A=
ENST00000546844.1:c.-95-70A= ENSP00000446658.1:n.-95-70A=
ENST00000547319.1:n.217-70A=
ENST00000551337.5:c.-95-70A= ENSP00000447620.1:n.-95-70A=
ENST00000553106.5:c.-165A= ENSP00000448059.1:n.-165A=
ENST00000635500.1:n.29-4397A=
NM_000277.1:c.-165A= NP_000268.1:n.-165A=
NM_000277.2:c.-165A= NP_000268.1:n.-165A=
NM_001354304.1:c.-95-70A= NP_001341233.1:n.-95-70A=
NM_001354304.2:c.-95-70A= NP_001341233.1:n.-95-70A=