Canonical Allele Identifier: CA2059445883
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843337G= , CM000674.2:g.102843337G= GRCh38
NC_000012.11:g.103237115G= , CM000674.1:g.103237115G= GRCh37
NC_000012.10:g.101761245G= NCBI36
NG_008690.1:g.79266C=
NG_008690.2:g.120074C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1199+309C= MANE Select ENSP00000448059.1:n.1199+309C=
ENST00000307000.7:c.1184+309C= ENSP00000303500.2:n.1184+309C=
ENST00000549247.6:n.958+309C=
ENST00000551114.2:n.861+309C=
ENST00000553106.5:c.1199+309C= ENSP00000448059.1:n.1199+309C=
ENST00000635477.1:c.303+309C=
ENST00000635528.1:n.714+309C=
NM_000277.1:c.1199+309C= NP_000268.1:n.1199+309C=
XM_011538422.1:c.1142+309C= XP_011536724.1:n.1142+309C=
NM_000277.2:c.1199+309C= NP_000268.1:n.1199+309C=
NM_001354304.1:c.1199+309C= NP_001341233.1:n.1199+309C=
NM_000277.3:c.1199+309C= MANE Select NP_000268.1:n.1199+309C=
NM_001354304.2:c.1199+309C= NP_001341233.1:n.1199+309C=