Canonical Allele Identifier: CA2059448427
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854711C= , CM000674.2:g.102854711C= GRCh38
NC_000012.11:g.103248489C= , CM000674.1:g.103248489C= GRCh37
NC_000012.10:g.101772619C= NCBI36
NG_008690.1:g.67892G=
NG_008690.2:g.108700G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.706+425G= MANE Select ENSP00000448059.1:n.706+425G=
ENST00000307000.7:c.691+425G= ENSP00000303500.2:n.691+425G=
ENST00000549111.5:n.1227G=
ENST00000553106.5:c.706+425G= ENSP00000448059.1:n.706+425G=
NM_000277.1:c.706+425G= NP_000268.1:n.706+425G=
XM_011538422.1:c.706+425G= XP_011536724.1:n.706+425G=
NM_000277.2:c.706+425G= NP_000268.1:n.706+425G=
NM_001354304.1:c.706+425G= NP_001341233.1:n.706+425G=
XM_017019370.2:c.*74G= XP_016874859.1:n.*74G=
NM_000277.3:c.706+425G= MANE Select NP_000268.1:n.706+425G=
NM_001354304.2:c.706+425G= NP_001341233.1:n.706+425G=