Canonical Allele Identifier: CA2059466585
Gene: PAH HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.329C= MANE Select ENSP00000448059.1:p.Ser110=
ENST00000307000.7:c.314C= ENSP00000303500.2:p.Ser105=
ENST00000546844.1:c.329C= ENSP00000446658.1:p.Ser110=
ENST00000548928.1:n.251C=
ENST00000549111.5:n.425C=
ENST00000550978.6:c.313C=
ENST00000551337.5:c.329C= ENSP00000447620.1:p.Ser110=
ENST00000551988.5:n.418C=
ENST00000553106.5:c.329C= ENSP00000448059.1:p.Ser110=
NM_000277.1:c.329C= NP_000268.1:p.Ser110=
XM_011538422.1:c.329C= XP_011536724.1:p.Ser110=
NM_000277.2:c.329C= NP_000268.1:p.Ser110=
NM_001354304.1:c.329C= NP_001341233.1:p.Ser110=
XM_017019370.2:c.329C= XP_016874859.1:p.Ser110=
NM_000277.3:c.329C= MANE Select NP_000268.1:p.Ser110=
NM_001354304.2:c.329C= NP_001341233.1:p.Ser110=