Canonical Allele Identifier: CA2059446051
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843488C= , CM000674.2:g.102843488C= GRCh38
NC_000012.11:g.103237266C= , CM000674.1:g.103237266C= GRCh37
NC_000012.10:g.101761396C= NCBI36
NG_008690.1:g.79115G=
NG_008690.2:g.119923G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1199+158G= MANE Select ENSP00000448059.1:n.1199+158G=
ENST00000307000.7:c.1184+158G= ENSP00000303500.2:n.1184+158G=
ENST00000549247.6:n.958+158G=
ENST00000551114.2:n.861+158G=
ENST00000553106.5:c.1199+158G= ENSP00000448059.1:n.1199+158G=
ENST00000635477.1:c.303+158G=
ENST00000635528.1:n.714+158G=
NM_000277.1:c.1199+158G= NP_000268.1:n.1199+158G=
XM_011538422.1:c.1142+158G= XP_011536724.1:n.1142+158G=
NM_000277.2:c.1199+158G= NP_000268.1:n.1199+158G=
NM_001354304.1:c.1199+158G= NP_001341233.1:n.1199+158G=
NM_000277.3:c.1199+158G= MANE Select NP_000268.1:n.1199+158G=
NM_001354304.2:c.1199+158G= NP_001341233.1:n.1199+158G=