Canonical Allele Identifier: CA2059449667
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855281C= , CM000674.2:g.102855281C= GRCh38
NC_000012.11:g.103249059C= , CM000674.1:g.103249059C= GRCh37
NC_000012.10:g.101773189C= NCBI36
NG_008690.1:g.67322G=
NG_008690.2:g.108130G=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.561G= MANE Select ENSP00000448059.1:p.Trp187=
ENST00000307000.7:c.546G= ENSP00000303500.2:p.Trp182=
ENST00000549111.5:n.657G=
ENST00000551988.5:n.582G=
ENST00000553106.5:c.561G= ENSP00000448059.1:p.Trp187=
NM_000277.1:c.561G= NP_000268.1:p.Trp187=
XM_011538422.1:c.561G= XP_011536724.1:p.Trp187=
NM_000277.2:c.561G= NP_000268.1:p.Trp187=
NM_001354304.1:c.561G= NP_001341233.1:p.Trp187=
XM_017019370.2:c.561G= XP_016874859.1:p.Trp187=
NM_000277.3:c.561G= MANE Select NP_000268.1:p.Trp187=
NM_001354304.2:c.561G= NP_001341233.1:p.Trp187=