Canonical Allele Identifier: CA2059448554
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844427T= , CM000674.2:g.102844427T= GRCh38
NC_000012.11:g.103238205T= , CM000674.1:g.103238205T= GRCh37
NC_000012.10:g.101762335T= NCBI36
NG_008690.1:g.78176A=
NG_008690.2:g.118984A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.974A= MANE Select ENSP00000448059.1:p.Tyr325=
ENST00000307000.7:c.959A= ENSP00000303500.2:p.Tyr320=
ENST00000549247.6:n.733A=
ENST00000551114.2:n.636A=
ENST00000553106.5:c.974A= ENSP00000448059.1:p.Tyr325=
ENST00000635477.1:c.78A=
ENST00000635528.1:n.489A=
NM_000277.1:c.974A= NP_000268.1:p.Tyr325=
XM_011538422.1:c.917A= XP_011536724.1:p.Tyr306=
NM_000277.2:c.974A= NP_000268.1:p.Tyr325=
NM_001354304.1:c.974A= NP_001341233.1:p.Tyr325=
NM_000277.3:c.974A= MANE Select NP_000268.1:p.Tyr325=
NM_001354304.2:c.974A= NP_001341233.1:p.Tyr325=