Canonical Allele Identifier: CA16020923
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1693237
ClinVar RCV Id: RCV002260496
dbSNP Id: rs2136636774

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844344del , CM000674.2:g.102844344del GRCh38
NC_000012.11:g.103238122del , CM000674.1:g.103238122del GRCh37
NC_000012.10:g.101762252del NCBI36
NG_008690.1:g.78259del
NG_008690.2:g.119067del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1057del MANE Select ENSP00000448059.1:p.Glu353AsnfsTer?
ENST00000307000.7:c.1042del ENSP00000303500.2:p.Glu348AsnfsTer?
ENST00000549247.6:n.816del
ENST00000551114.2:n.719del
ENST00000553106.5:c.1057del ENSP00000448059.1:p.Glu353AsnfsTer?
ENST00000635477.1:c.161del
ENST00000635528.1:n.572del
NM_000277.1:c.1057del NP_000268.1:p.Glu353AsnfsTer?
XM_011538422.1:c.1000del XP_011536724.1:p.Glu334AsnfsTer?
NM_000277.2:c.1057del NP_000268.1:p.Glu353AsnfsTer?
NM_001354304.1:c.1057del NP_001341233.1:p.Glu353AsnfsTer?
NM_000277.3:c.1057del MANE Select NP_000268.1:p.Glu353AsnfsTer?
NM_001354304.2:c.1057del NP_001341233.1:p.Glu353AsnfsTer?