Canonical Allele Identifier: CA2059445852
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843308G= , CM000674.2:g.102843308G= GRCh38
NC_000012.11:g.103237086G= , CM000674.1:g.103237086G= GRCh37
NC_000012.10:g.101761216G= NCBI36
NG_008690.1:g.79295C=
NG_008690.2:g.120103C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1199+338C= MANE Select ENSP00000448059.1:n.1199+338C=
ENST00000307000.7:c.1184+338C= ENSP00000303500.2:n.1184+338C=
ENST00000549247.6:n.958+338C=
ENST00000551114.2:n.861+338C=
ENST00000553106.5:c.1199+338C= ENSP00000448059.1:n.1199+338C=
ENST00000635477.1:c.303+338C=
ENST00000635528.1:n.714+338C=
NM_000277.1:c.1199+338C= NP_000268.1:n.1199+338C=
XM_011538422.1:c.1142+338C= XP_011536724.1:n.1142+338C=
NM_000277.2:c.1199+338C= NP_000268.1:n.1199+338C=
NM_001354304.1:c.1199+338C= NP_001341233.1:n.1199+338C=
NM_000277.3:c.1199+338C= MANE Select NP_000268.1:n.1199+338C=
NM_001354304.2:c.1199+338C= NP_001341233.1:n.1199+338C=