Canonical Allele Identifier: CA16020766
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 987778
ClinVar RCV Id: RCV001269078
dbSNP Id: rs1877424058

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894759_102894763del , CM000674.2:g.102894759_102894763del GRCh38
NC_000012.11:g.103288537_103288541del , CM000674.1:g.103288537_103288541del GRCh37
NC_000012.10:g.101812667_101812671del NCBI36
NG_008690.1:g.27840_27844del
NG_008690.2:g.68648_68652del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.324_328del MANE Select ENSP00000448059.1:p.Glu108AspfsTer4
ENST00000307000.7:c.309_313del ENSP00000303500.2:p.Glu103AspfsTer4
ENST00000546844.1:c.324_328del ENSP00000446658.1:p.Glu108AspfsTer4
ENST00000548928.1:n.246_250del
ENST00000549111.5:n.420_424del
ENST00000550978.6:c.308_312del
ENST00000551337.5:c.324_328del ENSP00000447620.1:p.Glu108AspfsTer4
ENST00000551988.5:n.413_417del
ENST00000553106.5:c.324_328del ENSP00000448059.1:p.Glu108AspfsTer4
NM_000277.1:c.324_328del NP_000268.1:p.Glu108AspfsTer4
XM_011538422.1:c.324_328del XP_011536724.1:p.Glu108AspfsTer4
NM_000277.2:c.324_328del NP_000268.1:p.Glu108AspfsTer4
NM_001354304.1:c.324_328del NP_001341233.1:p.Glu108AspfsTer4
XM_017019370.2:c.324_328del XP_016874859.1:p.Glu108AspfsTer4
NM_000277.3:c.324_328del MANE Select NP_000268.1:p.Glu108AspfsTer4
NM_001354304.2:c.324_328del NP_001341233.1:p.Glu108AspfsTer4