Canonical Allele Identifier: CA229507
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102645
dbSNP Id: rs62508682

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894804T>A , CM000674.2:g.102894804T>A GRCh38
NC_000012.11:g.103288582T>A , CM000674.1:g.103288582T>A GRCh37
NC_000012.10:g.101812712T>A NCBI36
NG_008690.1:g.27799A>T
NG_008690.2:g.68607A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.283A>T MANE Select ENSP00000448059.1:p.Ile95Phe
ENST00000307000.7:c.268A>T ENSP00000303500.2:p.Ile90Phe
ENST00000546844.1:c.283A>T ENSP00000446658.1:p.Ile95Phe
ENST00000548677.2:n.370A>T
ENST00000548928.1:n.205A>T
ENST00000549111.5:n.379A>T
ENST00000550978.6:c.267A>T
ENST00000551337.5:c.283A>T ENSP00000447620.1:p.Ile95Phe
ENST00000551988.5:n.372A>T
ENST00000553106.5:c.283A>T ENSP00000448059.1:p.Ile95Phe
NM_000277.1:c.283A>T NP_000268.1:p.Ile95Phe
XM_011538422.1:c.283A>T XP_011536724.1:p.Ile95Phe
NM_000277.2:c.283A>T NP_000268.1:p.Ile95Phe
NM_001354304.1:c.283A>T NP_001341233.1:p.Ile95Phe
XM_017019370.2:c.283A>T XP_016874859.1:p.Ile95Phe
NM_000277.3:c.283A>T MANE Select NP_000268.1:p.Ile95Phe
NM_001354304.2:c.283A>T NP_001341233.1:p.Ile95Phe