Canonical Allele Identifier: CA2059451271
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846896G= , CM000674.2:g.102846896G= GRCh38
NC_000012.11:g.103240674G= , CM000674.1:g.103240674G= GRCh37
NC_000012.10:g.101764804G= NCBI36
NG_008690.1:g.75707C=
NG_008690.2:g.116515C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.968C= MANE Select ENSP00000448059.1:p.Thr323=
ENST00000307000.7:c.953C= ENSP00000303500.2:p.Thr318=
ENST00000549247.6:n.727C=
ENST00000551114.2:n.630C=
ENST00000553106.5:c.968C= ENSP00000448059.1:p.Thr323=
ENST00000635477.1:c.74-2465C=
ENST00000635528.1:n.483C=
NM_000277.1:c.968C= NP_000268.1:p.Thr323=
XM_011538422.1:c.913-2465C= XP_011536724.1:n.913-2465C=
NM_000277.2:c.968C= NP_000268.1:p.Thr323=
NM_001354304.1:c.968C= NP_001341233.1:p.Thr323=
NM_000277.3:c.968C= MANE Select NP_000268.1:p.Thr323=
NM_001354304.2:c.968C= NP_001341233.1:p.Thr323=