Canonical Allele Identifier: CA180267
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102795
dbSNP Id: rs62508624

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852957T>A , CM000674.2:g.102852957T>A GRCh38
NC_000012.11:g.103246735T>A , CM000674.1:g.103246735T>A GRCh37
NC_000012.10:g.101770865T>A NCBI36
NG_008690.1:g.69646A>T
NG_008690.2:g.110454A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.707-7A>T MANE Select ENSP00000448059.1:n.707-7A>T
ENST00000307000.7:c.692-7A>T ENSP00000303500.2:n.692-7A>T
ENST00000549247.6:n.459A>T
ENST00000553106.5:c.707-7A>T ENSP00000448059.1:n.707-7A>T
NM_000277.1:c.707-7A>T NP_000268.1:n.707-7A>T
XM_011538422.1:c.707-7A>T XP_011536724.1:n.707-7A>T
NM_000277.2:c.707-7A>T NP_000268.1:n.707-7A>T
NM_001354304.1:c.707-7A>T NP_001341233.1:n.707-7A>T
NM_000277.3:c.707-7A>T MANE Select NP_000268.1:n.707-7A>T
NM_001354304.2:c.707-7A>T NP_001341233.1:n.707-7A>T