Canonical Allele Identifier: CA16041561
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 370308
ClinVar RCV Id: RCV000410526
dbSNP Id: rs1057516389

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894758del , CM000674.2:g.102894758del GRCh38
NC_000012.11:g.103288536del , CM000674.1:g.103288536del GRCh37
NC_000012.10:g.101812666del NCBI36
NG_008690.1:g.27845del
NG_008690.2:g.68653del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.329del MANE Select ENSP00000448059.1:p.Ser110TyrfsTer?
ENST00000307000.7:c.314del ENSP00000303500.2:p.Ser105TyrfsTer?
ENST00000546844.1:c.329del ENSP00000446658.1:p.Ser110TyrfsTer?
ENST00000548928.1:n.251del
ENST00000549111.5:n.425del
ENST00000550978.6:c.313del
ENST00000551337.5:c.329del ENSP00000447620.1:p.Ser110TyrfsTer?
ENST00000551988.5:n.418del
ENST00000553106.5:c.329del ENSP00000448059.1:p.Ser110TyrfsTer?
NM_000277.1:c.329del NP_000268.1:p.Ser110TyrfsTer?
XM_011538422.1:c.329del XP_011536724.1:p.Ser110TyrfsTer?
NM_000277.2:c.329del NP_000268.1:p.Ser110TyrfsTer?
NM_001354304.1:c.329del NP_001341233.1:p.Ser110TyrfsTer?
XM_017019370.2:c.329del XP_016874859.1:p.Ser110TyrfsTer?
NM_000277.3:c.329del MANE Select NP_000268.1:p.Ser110TyrfsTer?
NM_001354304.2:c.329del NP_001341233.1:p.Ser110TyrfsTer?