Canonical Allele Identifier: CA229312
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102499
dbSNP Id: rs62507350

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844345del , CM000674.2:g.102844345del GRCh38
NC_000012.11:g.103238123del , CM000674.1:g.103238123del GRCh37
NC_000012.10:g.101762253del NCBI36
NG_008690.1:g.78258del
NG_008690.2:g.119066del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1056del MANE Select ENSP00000448059.1:p.Glu353AsnfsTer?
ENST00000307000.7:c.1041del ENSP00000303500.2:p.Glu348AsnfsTer?
ENST00000549247.6:n.815del
ENST00000551114.2:n.718del
ENST00000553106.5:c.1056del ENSP00000448059.1:p.Glu353AsnfsTer?
ENST00000635477.1:c.160del
ENST00000635528.1:n.571del
NM_000277.1:c.1056del NP_000268.1:p.Glu353AsnfsTer?
XM_011538422.1:c.999del XP_011536724.1:p.Glu334AsnfsTer?
NM_000277.2:c.1056del NP_000268.1:p.Glu353AsnfsTer?
NM_001354304.1:c.1056del NP_001341233.1:p.Glu353AsnfsTer?
NM_000277.3:c.1056del MANE Select NP_000268.1:p.Glu353AsnfsTer?
NM_001354304.2:c.1056del NP_001341233.1:p.Glu353AsnfsTer?