Canonical Allele Identifier: CA2620510753
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917255G>T , CM000674.2:g.102917255G>T GRCh38
NC_000012.11:g.103311033G>T , CM000674.1:g.103311033G>T GRCh37
NC_000012.10:g.101835163G>T NCBI36
NG_008690.1:g.5348C>A
NG_008690.2:g.46156C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-30C>A
ENST00000546844.1:c.-95-30C>A ENSP00000446658.1:n.-95-30C>A
ENST00000547319.1:n.217-30C>A
ENST00000551337.5:c.-95-30C>A ENSP00000447620.1:n.-95-30C>A
ENST00000553106.5:c.-125C>A ENSP00000448059.1:n.-125C>A
ENST00000635500.1:n.29-4357C>A
NM_000277.1:c.-125C>A NP_000268.1:n.-125C>A
NM_000277.2:c.-125C>A NP_000268.1:n.-125C>A
NM_001354304.1:c.-95-30C>A NP_001341233.1:n.-95-30C>A
NM_001354304.2:c.-95-30C>A NP_001341233.1:n.-95-30C>A