Canonical Allele Identifier: CA2059466588
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894758_102894763delinsGAAAGC , CM000674.2:g.102894758_102894763delinsGAAAGC GRCh38
NC_000012.11:g.103288536_103288541delinsGAAAGC , CM000674.1:g.103288536_103288541delinsGAAAGC GRCh37
NC_000012.10:g.101812666_101812671delinsGAAAGC NCBI36
NG_008690.1:g.27840_27845delinsGCTTTC
NG_008690.2:g.68648_68653delinsGCTTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.324_329delinsGCTTTC MANE Select ENSP00000448059.1:p.Glu108=
ENST00000307000.7:c.309_314delinsGCTTTC ENSP00000303500.2:p.Glu103=
ENST00000546844.1:c.324_329delinsGCTTTC ENSP00000446658.1:p.Glu108=
ENST00000548928.1:n.246_251delinsGCTTTC
ENST00000549111.5:n.420_425delinsGCTTTC
ENST00000550978.6:c.308_313delinsGCTTTC
ENST00000551337.5:c.324_329delinsGCTTTC ENSP00000447620.1:p.Glu108=
ENST00000551988.5:n.413_418delinsGCTTTC
ENST00000553106.5:c.324_329delinsGCTTTC ENSP00000448059.1:p.Glu108=
NM_000277.1:c.324_329delinsGCTTTC NP_000268.1:p.Glu108=
XM_011538422.1:c.324_329delinsGCTTTC XP_011536724.1:p.Glu108=
NM_000277.2:c.324_329delinsGCTTTC NP_000268.1:p.Glu108=
NM_001354304.1:c.324_329delinsGCTTTC NP_001341233.1:p.Glu108=
XM_017019370.2:c.324_329delinsGCTTTC XP_016874859.1:p.Glu108=
NM_000277.3:c.324_329delinsGCTTTC MANE Select NP_000268.1:p.Glu108=
NM_001354304.2:c.324_329delinsGCTTTC NP_001341233.1:p.Glu108=