Canonical Allele Identifier: CA2059466579
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894757T= , CM000674.2:g.102894757T= GRCh38
NC_000012.11:g.103288535T= , CM000674.1:g.103288535T= GRCh37
NC_000012.10:g.101812665T= NCBI36
NG_008690.1:g.27846A=
NG_008690.2:g.68654A=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.330A= MANE Select ENSP00000448059.1:p.Ser110=
ENST00000307000.7:c.315A= ENSP00000303500.2:p.Ser105=
ENST00000546844.1:c.330A= ENSP00000446658.1:p.Ser110=
ENST00000548928.1:n.252A=
ENST00000549111.5:n.426A=
ENST00000550978.6:c.314A=
ENST00000551337.5:c.330A= ENSP00000447620.1:p.Ser110=
ENST00000551988.5:n.419A=
ENST00000553106.5:c.330A= ENSP00000448059.1:p.Ser110=
NM_000277.1:c.330A= NP_000268.1:p.Ser110=
XM_011538422.1:c.330A= XP_011536724.1:p.Ser110=
NM_000277.2:c.330A= NP_000268.1:p.Ser110=
NM_001354304.1:c.330A= NP_001341233.1:p.Ser110=
XM_017019370.2:c.330A= XP_016874859.1:p.Ser110=
NM_000277.3:c.330A= MANE Select NP_000268.1:p.Ser110=
NM_001354304.2:c.330A= NP_001341233.1:p.Ser110=